In the Epistulae ex ponto, Ovid describes how he dealt with the arrival of the silver images of Augustus, Livia and Tiberia that Cotta Messalinus sent him (2.8). He also described his sacrum Caesaris while celebrating the Pomponius brothers for attaining consulships (4.9). The theme of emperor worship as a medium of communication between patrons and their exiled client is striking. Millar noted how Ovid was kept informed of the metamorphoses of the imperial household (Millar 1993, 15-17), and Syme pointed to Ovid’s ability to useconcurrent language of homage at Rome(Syme 1978, 167-8). As such, Ovid’s descriptions bear significance beyond proving that domestic worship of living emperors and his household existed (Gradel 2002, 202-203; Martelli 2013, 200).
This paper argues that Ovid’s epistles show how elite Roman society cared about emperor worship. Ovid received the proper set of statues of the imperial family from his friend and patron Cotta Messalinus. He reported to the Pomponius brothers regarding how Tiberius and Livia stantpariter beside the deified Augustus in his sacrum Caesaris, and about his prayers that are meant for public consumption (Price 1984, 92). At stake is his hope to return to Rome: the proper exercise of worship demonstrates not only his pietas but also how he projected imperial symbolism on the edge of the empire. Hence, he boasted how Pontusknew of his pietas as part of his metric resumé submitted to his friend and patron Pomponius Graecinus (Helzle 1989, 22-26). Together with Pliny the Younger’s foundation of a temple at Tifernum (Ep. 10.8), the literary sources offer a potential model for the foundation process of small temples such as the one found at Eretria (Schmid 2001, 113), or others as documented by Simon Price (1984) and Heidi Hänlein-Schäfer (1985).
OBJECTIVES: We previously reported that compared with night sleep, day sleep among shift workers was associated with reduced urinary excretion of 8-hydroxydeoxyguanosine (8-OH-dG), potentially reflecting a reduced ability to repair 8-OH-dG lesions in DNA. We identified the absence of melatonin during day sleep as the likely causative factor. We now investigate whether night work is also associated with reduced urinary excretion of 8-OH-dG. METHODS: For this cross-sectional study, 50 shift workers with the largest negative differences in night work versus night sleep circulating melatonin levels (measured as 6-sulfatoxymelatonin in urine) were selected from among the 223 shift workers included in our previous study. 8-OH-dG concentrations were measured in stored urine samples using high performance liquid chromatography with electrochemical detection. Mixed effects models were used to compare night work versus night sleep 8-OH-dG levels. RESULTS: Circulating melatonin levels during night work (mean=17.1 ng/mg creatinine/mg creatinine) were much lower than during night sleep (mean=51.7 ng/mg creatinine). In adjusted analyses, average urinary 8-OH-dG levels during the night work period were only 20% of those observed during the night sleep period (95% CI 10% to 30%; p<0.001). CONCLUSIONS: This study suggests that night work, relative to night sleep, is associated with reduced repair of 8-OH-dG lesions in DNA and that the effect is likely driven by melatonin suppression occurring during night work relative to night sleep. If confirmed, future studies should evaluate melatonin supplementation as a means to restore oxidative DNA damage repair capacity among shift workers.
Xu C, Liu G, Zhao R, Yang S, Luo G, Zhang Z. A Parallel Bandit-Based Approach for Autotuning FPGA Compilation, in Proceedings of the 2017 ACM/SIGDA International Symposium on Field-Programmable Gate Arrays - FPGA '17. New York, New York, USA: ACM Press; 2017:157–166. 访问链接
Nutrients loading reduction in watershed is essential for lake restoration from eutrophication. The efficient and optimal decision-making on loading reduction is generally based on water quality modeling and the quantitative identification of nutrient sources at the watershed scale. The modeling process is influenced inevitably by inherent uncertainties, especially by uncertain parameters due to equifinality. Therefore, the emerging question is: if there is parameter uncertainty, how to ensure the robustness of the optimal decisions? Based on simulation-optimization models, an integrated approach of pattern identification and analysis of robustness was proposed in this study that focuses on the impact of parameter uncertainty in water quality modeling. Here the pattern represents the discernable regularity of solutions for load reduction under multiple parameter sets. Pattern identification is achieved by using a hybrid clustering analysis (i.e., Ward-Hierarchical and K-means), which was flexible and efficient in analyzing Lake Bali near the Yangtze River in China. The results demonstrated that urban domestic nutrient load is the most potential source that should be reduced, and there are two patterns for Total Nitrogen (TN) reduction and three patterns for Total Phosphorus (TP) reduction. The patterns indicated different total reduction of nutrient loads, which reflect diverse decision preferences. The robust solution was identified by the highest accomplishment with the water quality at monitoring stations that were improved uniformly with this solution. We conducted a process analysis of robust decision-making that was based on pattern identification and uncertainty, which provides effective support for decision making with preference under uncertainty. (C) 2017 Elsevier B.V. All rights reserved.
Chongqing, the largest megacity in southwest China, faces serious aerosol pollution but lacks information on particle characteristics and its sources. Official data released by Chongqing Environmental Protection Bureau demonstrated that urban PM10 concentrations decreased remarkably from 150 μg m− 3 in 2000 to 90 μg m− 3 in 2012. However, only several peer-reviewed studies paid attention to local fine particle (PM2.5) pollution. In the study, PM2.5 samples were obtained and subjected to chemical analysis in an urban site of the city during 2012 to 2013. The annual mean PM10 and PM2.5 concentrations in urban Chongqing were 103.9 ± 52.5 and 75.4 ± 42.2 μg m− 3, respectively. PM2.5 showed a distinct seasonality of high concentration in winter and similar levels in other seasons. The average OC/EC (organic carbon/element carbon) ratio was 3.7 with more high-OC/EC ratio sources contribution in autumn and winter. The varying sources and formation mechanisms resulted in SO42 − and NH4+ peaks in both summer and winter, whereas high nitrate concentration was only observed in winter. In the average mass closure, PM2.5 was composed of 23.0% SO42 −, 11.7% NO3−, 10.9% NH4+, 30.8% OM (organic matter), 5.2% EC, 8.2% mineral dust, 0.6% TEO (trace elements), 1.0% Cl− and 1.1% K+, while exhibiting large seasonal variability. Using positive matrix factorization (PMF), six sources were apportioned in PM2.5: secondary inorganic aerosols, coal combustion, other industrial pollution, soil dust, vehicular emission, and metallurgical industry. The annual mean contribution of above sources to PM2.5 was 37.5, 22.0, 17.5, 11.0, 9.8 and 2.2%, respectively. Coal combustion was identified by As tracer and dominated the primary sources of PM2.5, while the two different industrial sources were characterized by Cr and Mo, Co, Ni, and Se, respectively. The study is of great importance in characterizing the historical trends, current chemical characteristics and sources of fine particles in urban Chongqing.
Background: Previous studies have indicated that the cardioprotective effects of long-chain (LC) n-3 (omega-3) polyunsaturated fatty acids (PUFAs) may vary across various ethnic populations. Emerging evidence has suggested that the gene-environment interaction may partly explain such variations. Proprotein convertase subtilisin/kexin type 9 (PCSK9) was shown to have a mutually regulating relation with LC n-3 PUFAs and also to reduce the risk of cardiovascular diseases (CVDs). Therefore, we hypothesized that certain PCSK9 genetic variants may modify the association between LC n-3 PUFA intake and CVD risk.Objective: We determined whether a PCSK9 variant (rs11206510), which has been identified for early onset myocardial infarction (MI), modified the association of LC n-3 PUFAs with nonfatal MI risk in Costa Rican Hispanics.Design: We analyzed cross-sectional data from 1932 case subjects with a first nonfatal MI and 2055 population-based control subjects who were living in Costa Rica to examine potential gene-environment interactions. Two-sided P values <0.05 were considered significant.Results: We observed a significant interaction between the PCSK9 rs11206510 genotype and LC n-3 PUFA intake on nonfatal MI risk (P-interaction = 0.012). The OR of nonfatal MI was 0.84 (95% CI: 0.72, 0.98) per 0.1% increase in total energy intake from LC n-3 PUFAs in protective-allele (C-allele) carriers, whereas the corresponding OR (95% CI) in non-C-allele carriers was 1.02 (95% CI: 0.95, 1.10). Similar results were observed when we examined the association between docosahexaenoic acid, which is one type of LC n-3 PUFA, and nonfatal MI risk (P-interaction = 0.003).Conclusion: LC n-3 PUFA intake is associated with a lower risk of nonfatal MI in C-allele carriers of PCSK9 rs11206510 (n = 799) but not in non-C-allele carriers (n = 3188).
A further leakage reduction of AlGaN/GaN HEMTs with cap gate (CG-HEMTs) has been achieved by optimizing the gate structure and the gate etching process. The optimized CG-HEMTs single finger power HEMTs deliver IDSmax = 533 mA/mm at least with gate length of 0.5um and show a median gate leakage current of 20 nA/mm 25℃ measured at a drain voltage of 200 V. The breakdown voltage (BV) of CG-HEMTswas evaluated by the variation of drain-to-gate spacing (LDG) larger than 8 um. Furthermore, we show that the forward voltage of CG-HEMTs can be improved by shrinking the lateral dimension of the edge termination due to reduced series resistance.
The roles and characteristics of postzygotic single‐nucleotide mosaicisms (pSNMs) in autism spectrum disorders (ASDs) remain unclear. In this study of the whole exomes of 2,361 families in the Simons Simplex Collection, we identified 1,248 putative pSNMs in children and 285 de novo SNPs in children with detectable parental mosaicism. Ultra‐deep amplicon resequencing suggested a validation rate of 51%. Analyses of validated pSNMs revealed that missense/loss‐of‐function (LoF) pSNMs with a high mutant allele fraction (MAF≥ 0.2) contributed to ASD diagnoses (P = 0.022, odds ratio [OR] = 5.25), whereas missense/LoF pSNMs with a low MAF (MAF<0.2) contributed to autistic traits in male non‐ASD siblings (P = 0.033). LoF pSNMs in parents were less likely to be transmitted to offspring than neutral pSNMs (P = 0.037), and missense/LoF pSNMs in parents with a low MAF were transmitted more to probands than to siblings (P = 0.016, OR = 1.45). We estimated that pSNMs in probands or de novo mutations inherited from parental pSNMs increased the risk of ASD by approximately 6%. Adding pSNMs into the transmission and de novo association test model revealed 13 new ASD risk genes. These results expand the existing repertoire of genes involved in ASD and shed new light on the contribution of genomic mosaicisms to ASD diagnoses and autistic traits.
