Compost Carryover: Nitrogen Phosphorous and FT-IR Analysis of Soil Organic Matter

Compost plays a central role in organic soil fertility plans but is bulky and costly to apply. Determining compost carryover is therefore important for cost-effective soil fertility planning. This study investigated two aspects of nutritive carryover [nitrogen and phosphorus (P)], and an indicator of non-nutritive carryover [soil organic matter (SOM)] to determine the residual effect of a one-time compost application applied at four rates in a corn-squash rotation. Crop yield was measured as an integrated carryover indicator of nutritive and non-nutritive effects. Functional groups of compost and SOM were investigated using FT-IR spectroscopy and soil organic carbon (SOC). While year to year variability was great, compost had a persistent positive effect on crop yields, evident 3 years after application with no reduction in magnitude over time. Soil nitrate was low, and additions of compost at any rate generally did not increase levels beyond the year of application, with the exception of year four. Olsen P was also low, yet was higher in amended soils than in non-amended soils 3 years after application. Pronounced polysaccharide peaks, evident in compost spectra and absent in control soil, were apparent in compost-amended soils 3 years after compost treatment and SOC was greater 2 years afterwards. Compost carryover was most pronounced in year four following the incorporation of a nitrogen-fixing cover crop. These results show that compost can influence nutritive and non-nutritive soil properties many years after incorporation, thereby reinforcing the importance of including compost in organic fertility plans despite the unpredictability of year-to-year response

Cost-Driven Design of a Large Scale X-Plane

A conceptual design process focused on the development of a low-cost, large scale X-plane was developed as part of an internal research and development effort. One of the concepts considered for this process was the double-bubble configuration recently developed as an advanced single-aisle class commercial transport similar in size to a Boeing 737-800 or Airbus A320. The study objective was to reduce the contractor cost from contract award to first test flight to less than $100 million, and having the first flight within three years of contract award. Methods and strategies for reduced cost are discussed

Facial Curvature Detects and Explicates Ethnic Differences in Effects of Prenatal Alcohol Exposure

Background Our objective is to help clinicians detect the facial effects of prenatal alcohol exposure by developing computer-based tools for screening facial form. Methods All 415 individuals considered were evaluated by expert dysmorphologists and categorized as (i) healthy control (HC), (ii) fetal alcohol syndrome (FAS), or (iii) heavily prenatally alcohol exposed (HE) but not clinically diagnosable as FAS; 3D facial photographs were used to build models of facial form to support discrimination studies. Surface curvature-based delineations of facial form were introduced. Results (i) Facial growth in FAS, HE, and control subgroups is similar in both cohorts. (ii) Cohort consistency of agreement between clinical diagnosis and HC-FAS facial form classification is lower for midline facial regions and higher for nonmidline regions. (iii) Specific HC-FAS differences within and between the cohorts include: for HC, a smoother philtrum in Cape Coloured individuals; for FAS, a smoother philtrum in Caucasians; for control-FAS philtrum difference, greater homogeneity in Caucasians; for control-FAS face difference, greater homogeneity in Cape Coloured individuals. (iv) Curvature changes in facial profile induced by prenatal alcohol exposure are more homogeneous and greater in Cape Coloureds than in Caucasians. (v) The Caucasian HE subset divides into clusters with control-like and FAS-like facial dysmorphism. The Cape Coloured HE subset is similarly divided for nonmidline facial regions but not clearly for midline structures. (vi) The Cape Coloured HE subset with control-like facial dysmorphism shows orbital hypertelorism. Conclusions Facial curvature assists the recognition of the effects of prenatal alcohol exposure and helps explain why different facial regions result in inconsistent control-FAS discrimination rates in disparate ethnic groups. Heavy prenatal alcohol exposure can give rise to orbital hypertelorism, supporting a long-standing suggestion that prenatal alcohol exposure at a particular time causes increased separation of the brain hemispheres with a concomitant increase in orbital separation

Risk-based screening analysis of ground water contaminated by radionuclides introduced at the Nevada Test Site (NTS)

The Nevada Test Site (NTS) is located in the southwestern part of Nevada, about 105 km (65 mi) northwest of the city of Las Vegas. Underground tests of nuclear weapons devices have been conducted at the NTS since late 1962 and ground water beneath the NTS has been contaminated with radionuclides produced by these tests. This concern prompted this examination of the potential health risk to these individuals from drinking the contaminated ground water either at a location on the NTS (assuming loss of institutional control after 100 y) or at one offsite (considering groundwater migration). For the purpose of this assessment, a representative mix of the radionuclides of importance and their concentrations in ground water beneath the NTS were identified from measurements of radionuclide concentrations in groundwater samples-of-opportunity collected at the NTS. Transport of radionuclide-contaminated ground water offsite was evaluated using a travel-time-transport approach. At both locations of interest, potential human-health risk was calculated for an individual ingesting radionuclide-contaminated ground water over the course of a 70-y lifetime. Uncertainties about human physiological attributes, as well as about estimates of physical detriment per unit of radioactive material, were quantified and incorporated into the estimates of risk. The maximum potential excess lifetime risk of cancer mortality estimated for an individual at the offsite location ranges from 7 {times} 10{sup {minus}7} to 1 {times} 10{sup {minus}5}, and at the onsite location ranges from 3 {times} 10{sup {minus}3} to 2 {times} 10{sup {minus}2}. Both the offsite and the onsite estimates of risk are dominated by the lifetime doses from tritium. For the assessment of radionuclides in ground water, the critical uncertainty is their concentration today under the entire NTS

The Asymmetric Merger of Black Holes

We study event horizons of non-axisymmetric black holes and show how features found in axisymmetric studies of colliding black holes and of toroidal black holes are non-generic and how new features emerge. Most of the details of black hole formation and black hole merger are known only in the axisymmetric case, in which numerical evolution has successfully produced dynamical space-times. The work that is presented here uses a new approach to construct the geometry of the event horizon, not by locating it in a given spacetime, but by direct construction. In the axisymmetric case, our method produces the familiar pair-of-pants structure found in previous numerical simulations of black hole mergers, as well as event horizons that go through a toroidal epoch as discovered in the collapse of rotating matter. The main purpose of this paper is to show how new - substantially different - features emerge in the non-axisymmetric case. In particular, we show how black holes generically go through a toroidal phase before they become spherical, and how this fits together with the merger of black holes.Comment: 28 pages, 10 figures, uses REVTEX. Improved quality figures and additional color images are provided at http://www.phyast.pitt.edu/~shusa/EH

Utilization of HIV-1 envelope V3 to identify X4- and R5-specific Tat and LTR sequence signatures.

BACKGROUND: HIV-1 entry is a receptor-mediated process directed by the interaction of the viral envelope with the host cell CD4 molecule and one of two co-receptors, CCR5 or CXCR4. The amino acid sequence of the third variable (V3) loop of the HIV-1 envelope is highly predictive of co-receptor utilization preference during entry, and machine learning predictive algorithms have been developed to characterize sequences as CCR5-utilizing (R5) or CXCR4-utilizing (X4). It was hypothesized that while the V3 loop is predominantly responsible for determining co-receptor binding, additional components of the HIV-1 genome may contribute to overall viral tropism and display sequence signatures associated with co-receptor utilization. RESULTS: The accessory protein Tat and the HlV-1 long terminal repeat (LTR) were analyzed with respect to genetic diversity and compared by Jensen-Shannon divergence which resulted in a correlation with both mean genetic diversity as well as the absolute difference in genetic diversity between R5- and X4-genome specific trends. As expected, the V3 domain of the gp120 protein was enriched with statistically divergent positions. Statistically divergent positions were also identified in Tat amino acid sequences within the transactivation and TAR-binding domains, and in nucleotide positions throughout the LTR. We further analyzed LTR sequences for putative transcription factor binding sites using the JASPAR transcription factor binding profile database and found several putative differences in transcription factor binding sites between R5 and X4 HIV-1 genomes, specifically identifying the C/EBP sites I and II, and Sp site III to differ with respect to sequence configuration for R5 and X4 LTRs. CONCLUSION: These observations support the hypothesis that co-receptor utilization coincides with specific genetic signatures in HIV-1 Tat and the LTR, likely due to differing transcriptional regulatory mechanisms and selective pressures applied within specific cellular targets during the course of productive HIV-1 infection

Witten's 2+1 gravity on R x (Klein bottle)

Witten's formulation of 2+1 gravity is investigated on the nonorientable three-manifold R x (Klein bottle). The gauge group is taken to consist of all four components of the 2+1 Poincare group. We analyze in detail several components of the classical solution space, and we show that from four of the components one can recover nondegenerate spacetime metrics. In particular, from one component we recover metrics for which the Klein bottles are spacelike. An action principle is formulated for bundles satisfying a certain orientation compatibility property, and the corresponding components of the classical solution space are promoted into a phase space. Avenues towards quantization are briefly discussed.Comment: 33 pages, REVTeX v3.0, 3 figures in a separate PostScript fil

Biomarkers Predictive of Exacerbations in the SPIROMICS and COPDGene Cohorts

Rationale: Chronic obstructive pulmonary disease exacerbations are associated with disease progression, higher healthcare cost, and increased mortality. Published predictors of future exacerbations include previous exacerbation, airflow obstruction, poor overall health, home oxygen use, and gastroesophageal reflux

Diagnostic Delay Is Associated with Complicated Disease and Growth Impairment in Paediatric Crohn\u27s Disease

Background: Paediatric data on the association between diagnostic delay and inflammatory bowel disease [IBD] complications are lacking. We aimed to determine the effect of diagnostic delay on stricturing/fistulising complications, surgery, and growth impairment in a large paediatric cohort, and to identify predictors of diagnostic delay. Methods: We conducted a national, prospective, multicentre IBD inception cohort study including 1399 children. Diagnostic delay was defined as time from symptom onset to diagnosis \u3e75th percentile. Multivariable proportional hazards [PH] regression was used to examine the association between diagnostic delay and stricturing/fistulising complications and surgery, and multivariable linear regression to examine the association between diagnostic delay and growth. Predictors of diagnostic delay were identified using Cox PH regression. Results: Overall (64% Crohn\u27s disease [CD]; 36% ulcerative colitis/IBD unclassified [UC/IBD-U]; 57% male]), median time to diagnosis was 4.2 (interquartile range [IQR] 2.0-9.2) months. For the overall cohort, diagnostic delay was \u3e9.2 months; in CD, \u3e10.8 months and in UC/IBD-U, \u3e6.6 months. In CD, diagnostic delay was associated with a 2.5-fold higher rate of strictures/internal fistulae (hazard ratio [HR] 2.53, 95% confidence interval [CI] 1.41-4.56). Every additional month of diagnostic delay was associated with a decrease in height-for-age z-score of 0.013 standard deviations [95% CI 0.005-0.021]. Associations persisted after adjusting for disease location and therapy. No independent association was observed between diagnostic delay and surgery in CD or UC/IBD-U. Diagnostic delay was more common in CD, particularly small bowel CD. Abdominal pain, including isolated abdominal pain in CD, was associated with diagnostic delay. Conclusions: Diagnostic delay represents a risk factor for stricturing/internal fistulising complications and growth impairment in paediatric CD