101 research outputs found

    Present bias for monetary and dietary rewards: evidence from Chinese teenagers

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    Economists model self-control problems through time-inconsistent preferences. Empirical tests of these preferences largely rely on experimental elicitation methods using monetary rewards, with several recent studies failing to find present bias for money. In this paper, we compare estimates of present bias for money with estimates for healthy and unhealthy foods. In a within-subjects longitudinal experiment with 697 low-income Chinese high school students we find strong present bias for both money and food, and that individual measures of present bias are moderately correlated across reward types. Our experimental measures of time preferences over money predict field behaviours better than preferences elicited over foods

    Dominated Splitting and Pesin's Entropy Formula

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    Let MM be a compact manifold and f:MMf:\,M\to M be a C1C^1 diffeomorphism on MM. If μ\mu is an ff-invariant probability measure which is absolutely continuous relative to Lebesgue measure and for μ\mu a.e.xM,a.\,\,e.\,\,x\in M, there is a dominated splitting Torb(x)M=EFT_{orb(x)}M=E\oplus F on its orbit orb(x)orb(x), then we give an estimation through Lyapunov characteristic exponents from below in Pesin's entropy formula, i.e., the metric entropy hμ(f)h_\mu(f) satisfies hμ(f)χ(x)dμ,h_{\mu}(f)\geq\int \chi(x)d\mu, where χ(x)=i=1dimF(x)λi(x)\chi(x)=\sum_{i=1}^{dim\,F(x)}\lambda_i(x) and λ1(x)λ2(x)...λdimM(x)\lambda_1(x)\geq\lambda_2(x)\geq...\geq\lambda_{dim\,M}(x) are the Lyapunov exponents at xx with respect to μ.\mu. Consequently, by using a dichotomy for generic volume-preserving diffeomorphism we show that Pesin's entropy formula holds for generic volume-preserving diffeomorphisms, which generalizes a result of Tahzibi in dimension 2

    Steps and catalytic reactions: CO oxidation with preadsorbed O on Rh(553)

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    Industrial catalysts are often comprised of nanoparticles supported on high-surface-area oxides, in order to maximise the catalytically active surface area and thereby utilise the active material better. These nanoparticles expose steps and corners that, due to low coordination to neighboring atoms, are more reactive and, as a consequence, are often assumed to have higher catalytic activity. We have investigated the reaction between CO and preadsorbed O on a stepped Rh(553) surface, and show that CO oxidation indeed occurs faster than on the flat Rh(111) surface at the same temperature. However, we do find that this is not a result of reactions at the step sites but rather at the terrace sites close to the steps, due to in-plane relaxation enabled by the step. This insight can provide ways to optimize the shape of the nanoparticles to further improve the activity of certain reactions

    The gray matter volume of the amygdala is correlated with the perception of melodic intervals: a voxel-based morphometry study

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    Music is not simply a series of organized pitches, rhythms, and timbres, it is capable of evoking emotions. In the present study, voxel-based morphometry (VBM) was employed to explore the neural basis that may link music to emotion. To do this, we identified the neuroanatomical correlates of the ability to extract pitch interval size in a music segment (i.e., interval perception) in a large population of healthy young adults (N = 264). Behaviorally, we found that interval perception was correlated with daily emotional experiences, indicating the intrinsic link between music and emotion. Neurally, and as expected, we found that interval perception was positively correlated with the gray matter volume (GMV) of the bilateral temporal cortex. More important, a larger GMV of the bilateral amygdala was associated with better interval perception, suggesting that the amygdala, which is the neural substrate of emotional processing, is also involved in music processing. In sum, our study provides one of first neuroanatomical evidence on the association between the amygdala and music, which contributes to our understanding of exactly how music evokes emotional responses

    Development and validation of an ultra?performance liquid chromatography quadrupole time of flight mass spectrometry method for rapid quantification of free amino acids in human urine

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    An ultra-performance liquid chromatography quadrupole time of flight mass spectrometry (UPLC-qTOFMS)method using hydrophilic interaction liquid chromatography was developed and validated for simultaneous quantification of 18 free amino acids in urine with a total acquisition time including the column re-equilibration of less than 18 min per sample. This method involves simple sample preparation steps which consisted of 15 times dilution with acetonitrile to give a final composition of 25 % aqueous and 75 % acetonitrile without the need of any derivatization. The dynamic range for our calibration curve is approximately two orders of magnitude (120-fold from the lowest calibration curve point) with good linearity (r2 ? 0.995 for all amino acids). Good separation of all amino acids as well as good intra- and inter-day accuracy (<15 %) and precision (<15 %) were observed using three quality control samples at a concentration of low, medium and high range of the calibration curve. The limits of detection (LOD) and lower limit of quantification of our method were ranging from approximately 1–300 nM and 0.01–0.5 µM, respectively. The stability of amino acids in the prepared urine samples was found to be stable for 72 h at 4 °C, after one freeze thaw cycle and for up to 4 weeks at ?80 °C. We have applied this method to quantify the content of 18 free amino acids in 646 urine samples from a dietary intervention study. We were able to quantify all 18 free amino acids in these urine samples, if they were present at a level above the LOD. We found our method to be reproducible (accuracy and precision were typically <10 % for QCL, QCM and QCH) and the relatively high sample throughput nature of this method potentially makes it a suitable alternative for the analysis of urine samples in clinical setting
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