The Iowa State Capitol Grounds 1913 Extension and Reconstruction Project, October 2012

The Capitol grounds have been evolving through planned and unplanned actions for more than 150 years. The 1857 Constitutio established Des Moines as the capital. The commissioners appointed to choose a site decided on land donated by Wilson Alexander Scott and Harrison Lyon. Located on the east side of the Des Moines River, on a gently rising hill, the site for the Iowa State Capitol began with fewer than 10 acres. The Old Brick Capitol was built in the center of that 10-acre plot, and the area to the north was used as a public park until work began on the present day Capitol. In 1884, the two-year process of moving from the Old Brick Capitol to the new Capitol began. The state commissioned John Weidenman to design the first formal decoration of the grounds. Weidenman’s plans for the west approach to the Capitol included planting statues, and walkways. The State held some additional land but not necessarily land adjacent to the Capitol. In 1909, legislation was passed, and in 1913, the Thirty-Fifth General Assembly enacted controversial legislation to acquire additional land. A commission was formed to locate a purposed monument honoring the long-serving U.S. Senator William B. Allison. E.L. Masqueray was hired as the architect expert focusing on the selection of a proper site for the proposed Allison Memorial. Masqueray’s plan detailed the placement of buildings and potential monuments. Growth of the Capitol Complex, as known today, began.

Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways.

Through genome-wide association meta-analyses of up to 133,010 individuals of European ancestry without diabetes, including individuals newly genotyped using the Metabochip, we have increased the number of confirmed loci influencing glycemic traits to 53, of which 33 also increase type 2 diabetes risk (q < 0.05). Loci influencing fasting insulin concentration showed association with lipid levels and fat distribution, suggesting impact on insulin resistance. Gene-based analyses identified further biologically plausible loci, suggesting that additional loci beyond those reaching genome-wide significance are likely to represent real associations. This conclusion is supported by an excess of directionally consistent and nominally significant signals between discovery and follow-up studies. Functional analysis of these newly discovered loci will further improve our understanding of glycemic control.

Genome-wide association study identifies eight loci associated with blood pressure.

Elevated blood pressure is a common, heritable cause of cardiovascular disease worldwide. To date, identification of common genetic variants influencing blood pressure has proven challenging. We tested 2.5 million genotyped and imputed SNPs for association with systolic and diastolic blood pressure in 34,433 subjects of European ancestry from the Global BPgen consortium and followed up findings with direct genotyping (N ≤ 71,225 European ancestry, N ≤ 12,889 Indian Asian ancestry) and in silico comparison (CHARGE consortium, N = 29,136). We identified association between systolic or diastolic blood pressure and common variants in eight regions near the CYP17A1 (P = 7 × 10(-24)), CYP1A2 (P = 1 × 10(-23)), FGF5 (P = 1 × 10(-21)), SH2B3 (P = 3 × 10(-18)), MTHFR (P = 2 × 10(-13)), c10orf107 (P = 1 × 10(-9)), ZNF652 (P = 5 × 10(-9)) and PLCD3 (P = 1 × 10(-8)) genes. All variants associated with continuous blood pressure were associated with dichotomous hypertension. These associations between common variants and blood pressure and hypertension offer mechanistic insights into the regulation of blood pressure and may point to novel targets for interventions to prevent cardiovascular disease.

Improved Aggregate Gradation for Portland Cement Concrete Mixes, HR-563, 1996

Improving the aggregate gradation for a portland cement concrete mix may result in higher compressive strengths. With an improved gradation, the cement factor may be reduced to achieve a more economical concrete mix since cement is the most expensive component in a Portland cement concrete mix. This project located on I-80 westbound in Scott County, Iowa examined three different mixes. 1. Standard Class C mix with project aggregates. 2. Standard Class C mix with an improved aggregate gradation. 3. Standard Class C mix with an improved aggregate gradation and 10% cementitious reduction.

Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution.

To identify genetic loci influencing central obesity and fat distribution, we performed a meta-analysis of 16 genome-wide association studies (GWAS, N = 38,580) informative for adult waist circumference (WC) and waist-hip ratio (WHR). We selected 26 SNPs for follow-up, for which the evidence of association with measures of central adiposity (WC and/or WHR) was strong and disproportionate to that for overall adiposity or height. Follow-up studies in a maximum of 70,689 individuals identified two loci strongly associated with measures of central adiposity; these map near TFAP2B (WC, P = 1.9x10(-11)) and MSRA (WC, P = 8.9x10(-9)). A third locus, near LYPLAL1, was associated with WHR in women only (P = 2.6x10(-8)). The variants near TFAP2B appear to influence central adiposity through an effect on overall obesity/fat-mass, whereas LYPLAL1 displays a strong female-only association with fat distribution. By focusing on anthropometric measures of central obesity and fat distribution, we have identified three loci implicated in the regulation of human adiposity.

Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.

Concentrations of liver enzymes in plasma are widely used as indicators of liver disease. We carried out a genome-wide association study in 61,089 individuals, identifying 42 loci associated with concentrations of liver enzymes in plasma, of which 32 are new associations (P = 10(-8) to P = 10(-190)). We used functional genomic approaches including metabonomic profiling and gene expression analyses to identify probable candidate genes at these regions. We identified 69 candidate genes, including genes involved in biliary transport (ATP8B1 and ABCB11), glucose, carbohydrate and lipid metabolism (FADS1, FADS2, GCKR, JMJD1C, HNF1A, MLXIPL, PNPLA3, PPP1R3B, SLC2A2 and TRIB1), glycoprotein biosynthesis and cell surface glycobiology (ABO, ASGR1, FUT2, GPLD1 and ST3GAL4), inflammation and immunity (CD276, CDH6, GCKR, HNF1A, HPR, ITGA1, RORA and STAT4) and glutathione metabolism (GSTT1, GSTT2 and GGT), as well as several genes of uncertain or unknown function (including ABHD12, EFHD1, EFNA1, EPHA2, MICAL3 and ZNF827). Our results provide new insight into genetic mechanisms and pathways influencing markers of liver function.

Influência de porta-enxertos no crescimento de clones de seringueira no Estado de São Paulo

Este trabalho foi instalado na Estação Experimental de Agronomia de Pindorama, SP, com a finalidade de avaliar a interação enxerto vs. porta-enxertos de seringueira, Hevea brasiliensis (Willd. ex Adr. de Juss.) Müell. Arg. Os clones utilizados foram IAN 873, RRIM 600, RRIM 701, PB 235, PR 107 e GT 1, enxertados em seis diferentes porta-enxertos provenientes de sementes ilegítimas dos clones IAN 873, RRIM 600, RRIM 701, PB 235, GT 1 e de sementes não selecionadas. O delineamento utilizado foi o de blocos ao acaso, com parcelas subdivididas, tendo os porta-enxertos como tratamentos e os clones (enxertos) como subtratamentos, em quatro repetições. Os resultadosmostram que no período de avaliação o porta-enxerto GT 1 e IAN 873 foram os que produziram os maiores perímetros por planta, sendo 10,20 % maior que o de sementes não selecionadas. Paralelamente, os enxertos em vigor mostraram que os clones PB 235, RRIM 600 e PR 107 apresentaram melhor desempenho, com um perímetro do caule 8,12% maior que o dos clonesRRIM 701 e GT 1,notadamente os de menor vigor. A interação enxerto vs. porta-enxerto não foi significativa.

Islands of euchromatin-like sequence and expressed polymorphic sequences within the short arm of human chromosome 21.

The goals of the human genome project did not include sequencing of the heterochromatic regions. We describe here an initial sequence of 1.1 Mb of the short arm of human chromosome 21 (HSA21p), estimated to be 10% of 21p. This region contains extensive euchromatic-like sequence and includes on average one transcript every 100 kb. These transcripts show multiple inter- and intrachromosomal copies, and extensive copy number and sequence variability. The sequencing of the "heterochromatic" regions of the human genome is likely to reveal many additional functional elements and provide important evolutionary information.

Interactions of dietary whole-grain intake with fasting glucose- and insulin-related genetic loci in individuals of European descent: a meta-analysis of 14 cohort studies.

Whole-grain foods are touted for multiple health benefits, including enhancing insulin sensitivity and reducing type 2 diabetes risk. Recent genome-wide association studies (GWAS) have identified several single nucleotide polymorphisms (SNPs) associated with fasting glucose and insulin concentrations in individuals free of diabetes. We tested the hypothesis that whole-grain food intake and genetic variation interact to influence concentrations of fasting glucose and insulin. Via meta-analysis of data from 14 cohorts comprising ∼ 48,000 participants of European descent, we studied interactions of whole-grain intake with loci previously associated in GWAS with fasting glucose (16 loci) and/or insulin (2 loci) concentrations. For tests of interaction, we considered a P value <0.0028 (0.05 of 18 tests) as statistically significant. Greater whole-grain food intake was associated with lower fasting glucose and insulin concentrations independent of demographics, other dietary and lifestyle factors, and BMI (β [95% CI] per 1-serving-greater whole-grain intake: -0.009 mmol/l glucose [-0.013 to -0.005], P < 0.0001 and -0.011 pmol/l [ln] insulin [-0.015 to -0.007], P = 0.0003). No interactions met our multiple testing-adjusted statistical significance threshold. The strongest SNP interaction with whole-grain intake was rs780094 (GCKR) for fasting insulin (P = 0.006), where greater whole-grain intake was associated with a smaller reduction in fasting insulin concentrations in those with the insulin-raising allele. Our results support the favorable association of whole-grain intake with fasting glucose and insulin and suggest a potential interaction between variation in GCKR and whole-grain intake in influencing fasting insulin concentrations.

Avaliação de métodos de correção do estande para estimar a produtividade em milho

Este trabalho objetivou determinar o método de correção de estande mais adequado aos dados de produtividade na cultura do milho, na avaliação de 33 cultivares, em oito ambientes. Os métodos avaliados foram: sem correção, regra de três, método de Zuber, covariância de estande médio, covariância de estande ideal, o método proposto por Cruz, o método proposto por Vencovsky & Cruz, e o proposto neste trabalho, de correção estratificada com base no agrupamento de cultivares, para a característica estande, pelo teste de Scott & Knott. O método proposto neste trabalho, o de covariância de estande ideal e o de Vencovsky & Cruz foram mais adequados para essa correção, pois apresentaram baixos valores de coeficiente de variação e altos valores de F, confirmados pelos baixos valores de Pi e Pi multivariado na análise conjunta. Os métodos de regra de três e o proposto por Cruz apresentaram as maiores médias de produção, o que superestima o valor real da produção média. O método proposto neste trabalho foi eficiente em corrigir as cultivares, uma vez que as cultivares mais produtivas foram também as de maior potencial em deixar descendentes, medido pelo estande médio.

08024-14 Duck Creek Watershed Final Report

River Action is requesting funds for a project that offers design, technical and financial assistance to residential and commercial landowners and municipalities for the installation of buffers along Duck Creek and its tributaries. The buffers will improve water quality, reduce erosion on stream banks and provide habitat for wildlife. The projects will be planned and implemented through public meetings and educational workshops. This method of community involvement will increase awareness and education concerning the impairments in Duck Creek in Davenport and Bettendorf in Scott County, Iowa and promote personal responsibility and stewardship of watersheds.

Caracterização fenotípica e genotípica de progênies de pupunheira para palmito

A pupunheira (Bactris gasipaes H.B.K.) é considerada a espécie com maior potencial de produção de palmitos, em substituição aos tradicionais açaí (Euterpe oleracea Mart.) e juçara (Euterpe edulis Mart.). Os objetivos deste trabalho foram estimar alguns parâmetros genéticos associados à avaliação de 31 progênies de meios-irmãos de pupunheiras e classificar as melhores progênies pelo teste de médias de Scott-Knott. O delineamento experimental usado foi o de blocos ao acaso com três repetições, com parcelas experimentais de cinco plantas. As avaliações dos caracteres de altura da planta no momento do corte (APC), diâmetro da planta na altura do colo (DPC) e peso do palmito líquido (PPL) foram realizadas aos 15, 26 e 37 meses após o plantio. A população avaliada apresentou variação genética disponível para seleção e não sofreu efeito de interação com os cortes; o caráter PPL deverá ser testado com maior número de repetições, sendo o caráter mais sensível a efeitos de cortes; a razão entre o coeficiente de variação genética e o coeficiente de variação do erro indica que existem dificuldades nos processos de seleção nos caracteres avaliados; a correlação genotípica entre os caracteres DPC e PPL apresenta-se promissora para facilitar a seleção indireta do caráter PPL pelo caráter DPC. O agrupamento de médias de Scott-Knott classificou as progênies em dois grupos.

Does CRP Play a Causal Role in the Development of Coronary Heart Disease: Results of a Mendelian Randomisation Experiment Involving 128,935 People

Background: C-reactive protein (CRP) is associated with risk of coronary heart disease (CHD). Whether CRP is causally associated with CHD or merely a marker of underlying atherosclerosis is uncertain. Methods: We used a Mendelian randomisation design to investigate the causal relationship of CRP with CHD. We identified three genetic variants in the CRP locus (rs7553007, rs1130864 and rs1205) which influence CRP levels. We tested the three SNPs for association with CHD amongst 28,112 CHD cases and 100,823 controls. We then compared the observed relationship between the SNPs and CHD, with that predicted from the association of SNPs with CRP levels, and of CRP levels with CHD. Results: SNPs in the CRP locus were not associated with CHD: rs7553007, OR 0.98 (95% CI, 0.94-1.01); rs1130864, OR 1.00 (95% CI, 0.86-1.15); rs1205, OR 1.03 (95% CI, 0.99-1.07); combined OR for all three SNPs, 1.00 (95% CI, 0.97-1.02), per 20% lower CRP (figure). In contrast, the predicted OR for CHD from a 20% lower CRP level is 0.94 (95% CI, 0.94- 0.95), based on meta-analysis of observational studies. Conclusions: Though CRP variants are associated with CRP levels, and CRP levels with risk of CHD, we observed that CRP variants are not associated with CHD risk. Our Mendelian randomisation experiment strongly argues against a causal association of CRP with CHD.