Assessing long-term pH change in an Australian river catchment using monitoring and palaeolimnological data

Reviews of stream monitoring data suggest that there has been significant acidification (>1.0 pH unit at some sites) of Victorian streamwaters over the past 3 decades. To assess whether these declines are within the range of natural variability, we developed a diatom model for inferring past pH and applied it to a ca. 3500-yr diatom record from a flood plain lake, Callemondah 1 Billabong, on the Goulburn River, which has among the most substantial observed pH declines. The model has a jackkniffed r2 between diatom inferred and measured pH of 0.77 and a root mean square error of prediction of 0.35 pH units. In the pre-European period, pH was stable (range 6.5-6.7) for approximately 3000 yr. Since European settlement around 160 yr ago, diatom-inferred billabong pH has increased significantly by >0.5 units. We hypothesize that this increase in pH is related to processes associated with land clearance (e.g., increased base cation load and decreased organic acid load). There is no evidence of the recent monitored declines in the Callemondah record, which may indicate that that flood plain lakes and the main stream are experiencing divergent pH trends or that the temporal resolution in the billabong sediment record is insufficient to register recent declines.     

Temperature‐Dependent Exciton and Trap‐Related Photoluminescence of CdTe Quantum Dots Embedded in a NaCl Matrix: Implication in Thermometry

Temperature‐dependent optical studies of semiconductor quantum dots (QDs) are fundamentally important for a variety of sensing and imaging applications. The steady‐state and time‐resolved photoluminescence properties of CdTe QDs in the size range from 2.3 to 3.1 nm embedded into a protective matrix of NaCl are studied as a function of temperature from 80 to 360 K. The temperature coefficient is found to be strongly dependent on QD size, with the highest sensitivity obtained for the smallest size of QDs. The emission from solid‐state CdTe QD‐based powders is maintained with high color purity over a wide range of temperatures. Photoluminescence lifetime data suggest that temperature dependence of the intrinsic radiative lifetime in CdTe QDs is rather weak, and it is mostly the temperature‐dependent nonradiative decay of CdTe QDs which is responsible for the thermal quenching of photoluminescence intensity. By virtue of the temperature‐dependent photoluminescence behavior, high color purity, photostability, and high photoluminescence quantum yield (26%–37% in the solid state), CdTe QDs embedded in NaCl matrices are useful solid‐state probes for thermal imaging and sensing over a wide range of temperatures within a number of detection schemes and outstanding sensitivity, such as luminescence thermochromic imaging, ratiometric luminescence, and luminescence lifetime thermal sensing.     

Infrared-emitting colloidal nanocrystals: synthesis, assembly, spectroscopy, and applications

Semiconductor nanocrystals produced by means of colloidal chemistry in a solvent medium are an attractive class of nanometer-sized building blocks from which to create complex materials with unique properties for a variety of applications. Their optical and electronic properties can be tailored easily, both by their chemical composition and particle size. While colloidal nanocrystals emitting in the infrared region have seen a burst of attention during the last decade there is clearly a paucity of review articles covering their synthesis, assembly, spectroscopic characterization, and applications. This Review comprehensively addresses these topics for II-VI, III-V, and IV-VI nanocrystals, examples being HgTe and Cd(x)Hg(1-) (x)Te, InP and InAs, and PbS, PbSe, and PbTe, respectively. Among the applications discussed here are optical amplifier media for telecommunications systems, electroluminescence devices, and noninvasive optical imaging in biology.     

The intergenerational cycle of teenage motherhood: An ecological approach.

Objective: Daughters of teenage mothers have increased risk for teenage childbearing, perpetuating intergenerational cycles. Using Ecological Systems Theory, this study prospectively examined risk factors for teenage childbearing among a national sample of adolescent girls. Design: Data came from the National Longitudinal Survey of Youth 1997. Participants (N = 1,430) were recruited in early adolescence and interviewed yearly for 6 years. Survival analysis was used to examine the rate of childbirth across the teenage years by maternal age at first birth. Hierarchical Cox regression was used to identify multivariate predictors of teenage childbearing and to test whether risk factors differed between daughters of teenage versus older mothers. Primary Outcome Measure: Age at first childbirth was based on cumulative information collected at yearly interviews. Results: Daughters of teenage mothers were 66% more likely to become teenage mothers, after accounting for other risks. Individual (school performance), family (maternal education, marital status, number of children), peer (dating history), and environmental (race, enrichment) factors predicted teenage childbearing. Risks unique to daughters of teenage mothers were deviant peer norms, low parental monitoring, Hispanic race, and poverty. Conclusion: Results support multidimensional approaches to pregnancy prevention, and targeted interventions addressing unique risk factors among daughters of teenage mothers. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Use of colloidal ruthenium particles in the electrochemical reduction of benzene by solvated electrons

Ruthenium colloidal particles prepared by the decomposition of a ruthenium acid sulfite complex increased the electrochemical reduction of benzene from 45% to 60% at room temperature and 10 psig of hydrogen. The reduction was carried out in a 21 mole % ethanol - 79 mole % hexamethylphosporamide. The significant increase in the percent of benzene reduced was accompanied by an apparent current efficiency of 98%. Comparison with analogous experiments employing colloidal platinum particles indicates that the above increase in benzene reduction can be attributed to direct catalytic hydrogenation by the ruthenium.