‘Wiggle Matching’ Radiocarbon Dates

This paper covers three different methods of matching radiocarbon dates to the ‘wiggles’ of the calibration curve in those situations where the age difference between the 14C dates is known. These methods are most often applied to tree-ring sequences. The simplest approach is to use a classical Chi-squared fit of the 14C data to the 14C curve. This gives the calendar date where the data fit best and allows tests of how good the fit is. The only drawback of this method is that it is difficult to ascertain the uncertainty in the date found in this way. An extension of this technique uses a Monte-Carlo simulation to sample possible 14C concentrations consistent with the measurement made and for each of these possibilities performs a Chi-squared fit. This method yields a distribution of values in the calendrical time-scale, from which the overall dating uncertainty can be derived. A third, rather different approach, based on Bayesian statistics, calculates the relative likelihood of each possible calendar year fit. This can then be used to calculate a range of most likely dates in a similar way to the probability method of 14C calibration. The theories underlying all three methods are discussed in this paper and a comparison made for the fitting of specific model sequences. All three methods are found to give consistent results and the application of any one of them depends on the nature of the scientific question being addressed

Imaging dielectric relaxation in nanostructured polymers by frequency modulation electrostatic force microscopy

We have developed a method for imaging the temperature-frequency dependence of the dynamics of nanostructured polymer films with spatial resolution. This method provides images with dielectric compositional contrast well decoupled from topography. Using frequency-modulation electrostatic-force-microscopy, we probe the local frequency-dependent (0.1–100 Hz) dielectric response through measurement of the amplitude and phase of the force gradient in response to an oscillating applied electric field. When the phase is imaged at fixed frequency, it reveals the spatial variation in dielectric losses, i.e., the spatial variation in molecular/dipolar dynamics, with 40 nm lateral resolution. This is demonstrated by using as a model system; a phase separated polystyrene/polyvinyl-acetate (PVAc) blend. We show that nanoscale dynamic domains of PVAc are clearly identifiable in phase images as those which light-up in a band of temperature, reflecting the variations in the molecular/dipolar dynamics approaching the glass transition temperature of PVAc

The role of solar forcing upon climate change

Evidence for millennial-scale climate changes during the last 60,000 years has been found in Greenland ice cores and North Atlantic ocean cores. Until now, the cause of these climate changes remained a matter of debate. We argue that variations in solar activity may have played a significant role in forcing these climate changes. We review the coincidence of variations in cosmogenic isotopes (14C and 10Be) with climate changes during the Holocene and the upper part of the last Glacial, and present two possible mechanisms (involving the role of solar UV variations and solar wind/cosmic rays) that may explain how small variations in solar activity are amplified to cause significant climate changes. Accepting the idea of solar forcing of Holocene and Glacial climatic shifts has major implications for our view of present and future climate. It implies that the climate system is far more sensitive to small variations in solar activity than generally believed.

Interaction of Cupidin/Homer2 with two actin cytoskeletal regulators, Cdc42 small GTPase and Drebrin, in dendritic spines

<p>Abstract</p> <p>Background</p> <p>Homer is a postsynaptic scaffold protein that links various synaptic signaling proteins, including the type I metabotropic glutamate receptor subunits 1α and 5, the inositol 1,4,5-trisphosphate receptor, Shank and Cdc42 small GTPase. Overexpression of Homer induces changes in dendritic spine morphology in cultured hippocampal neurons. However, the molecular basis underpinning Homer-mediated spine morphogenesis remains unclear. In this study, we aimed to elucidate the structural and functional properties of the interaction between Cupidin/Homer2 and two actin-cytoskeletal regulators, Cdc42 small GTPase and Drebrin.</p> <p>Results</p> <p>Cupidin/Homer2 interacted with activated Cdc42 small GTPase via the Cdc42-binding domain that resides around amino acid residues 191–283, within the C-terminal coiled-coil domain. We generated a Cupidin deletion mutant lacking amino acids 191–230 (CPDΔ191–230), which showed decrease Cdc42-binding ability but maintained self-multimerization ability. Cupidin suppressed Cdc42-induced filopodia-like protrusion formation in HeLa cells, whereas CPDΔ191–230 failed to do so. In cultured hippocampal neurons, Cupidin was targeted to dendritic spines, whereas CPDΔ191–230 was distributed in dendritic shafts as well as spines. Overexpression of CPDΔ191–230 decreased the number of synapses and reduced the amplitudes of miniature excitatory postsynaptic currents in hippocampal neurons. Cupidin interacted with a dendritic spine F-actin-binding protein, Drebrin, which possesses two Homer ligand motifs, via the N-terminal EVH-1 domain. CPDΔ191–230 overexpression decreased Drebrin clustering in the dendritic spines of hippocampal neurons.</p> <p>Conclusion</p> <p>These results indicate that Cupidin/Homer2 interacts with the dendritic spine actin regulators Cdc42 and Drebrin via its C-terminal and N-terminal domains, respectively, and that it may be involved in spine morphology and synaptic properties.</p