Estimated Groundwater Withdrawals from Principal Aquifers in the United States, 2015

In 2015, about 84,600 million gallons per day (Mgal/d) of groundwater were withdrawn in the United States for various uses including public supply, self-supplied domestic, industrial, mining, thermoelectric power, aquaculture, livestock, and irrigation. Of this total, about 94 percent (79,200 Mgal/d) was withdrawn from principal aquifers, which are defined as regionally extensive aquifers or aquifer systems that have the potential to be used as sources of water of suitable quality and quantity to meet various needs. The remaining 6 percent (5,400 Mgal/d) was withdrawn from other, nonprincipal aquifers in the United States. Sixty-six principal aquifers belonging to 5 major lithologic groups have been identified and delineated in the United States, including Puerto Rico and the U.S. Virgin Islands. Of the water withdrawn from principal aquifers in 2015, 81 percent (63,900 Mgal/d) was from the unconsolidated and semiconsolidated sand and gravel lithologic group, 7.1 percent (5,630 Mgal/d) was from the igneous and metamorphic-rock lithologic group, 6.8 percent (5,360 Mgal/d) was from the carbonate-rock lithologic group, 3.4 percent (2,680 Mgal/d) was from the sandstone lithologic group, and 2.2 percent (1,710 Mgal/d) was from the sandstone and carbonate-rock lithologic group. The most heavily pumped of the 24 principal aquifers and aquifer systems within the unconsolidated and semiconsolidated sand and gravel lithologic group were the High Plains aquifer (12,300 Mgal/d), Mississippi River Valley alluvial aquifer (12,100 Mgal/d), Central Valley aquifer system (11,100 Mgal/d), and Basin and Range basin-fill aquifers (7,390 Mgal/d). Withdrawals for irrigation were 48,100 Mgal/d and accounted for 75 percent of the total withdrawals from this lithologic group. Although unconsolidated sand and gravel aquifers are widely distributed and were used as sources of water in all States except Hawaii and the U.S. Virgin Islands, 56 percent of the total withdrawn from unconsolidated and semiconsolidated sand and gravel aquifers was in just four States: California (15,600 Mgal/d), Arkansas (9,560 Mgal/d), Nebraska (5,570 Mgal/d), and Texas (4,830 Mgal/d). The most heavily pumped of the seven principal aquifers within the igneous and metamorphic-rock lithologic group were the Snake River Plain (2,930 Mgal/d) and Columbia Plateau basaltic-rock aquifers (1,080 Mgal/d), which are located in the northwestern United States and together accounted for 71 percent of the water withdrawn from this lithologic group. Withdrawals for irrigation were 4,190 Mgal/d and accounted for more than 74 percent of the total withdrawals from this lithologic group. Seventy-eight percent of the withdrawals from igneous and metamorphic-rock aquifers were in three States: Idaho (3,230 Mgal/d), Washington (614 Mgal/d), and Oregon (528 Mgal/d). The most heavily pumped of the 15 principal aquifers and aquifer systems within the carbonate-rock lithologic group were the Floridan aquifer system (3,180 Mgal/d) and the Biscayne aquifer (679 Mgal/d), which are in the southeastern United States and together accounted for almost 72 percent of the withdrawals from this lithologic group. Withdrawals for public supply (2,440 Mgal/d) and irrigation (1,610 Mgal/d) together accounted for almost 76 percent of the total withdrawals from this lithologic group. Although water was withdrawn from carbonate-rock aquifers in 35 States, 71 percent of the total withdrawn was in Florida (3,020 Mgal/d) and Georgia (785 Mgal/d). The most heavily pumped of the 15 principal aquifers within the sandstone lithologic group was the Cambrian- Ordovician aquifer system (921 Mgal/d), which is in the north-central United States and accounted for 34 percent of the water withdrawn from this lithologic group. Withdrawals for public supply were 1,030 Mgal/d and accounted for 38 percent of the total withdrawals from this lithologic group. Although sandstone aquifers were used as sources of water in 32 States, 45 percent of the total withdrawn from sandstone aquifers was in five States: Minnesota (321 Mgal/d), Wisconsin (319 Mgal/d), Kansas (193 Mgal/d), Illinois (187 Mgal/d), and Pennsylvania (179 Mgal/d). The most heavily pumped of the five principal aquifers and aquifer systems within the sandstone and carbonate rock lithologic group were the Edwards-Trinity aquifer system (661 Mgal/d) in the south-central United States and the Valley and Ridge aquifers (551 Mgal/d) of the eastern United States, which together accounted for 71 percent of total withdrawals from this lithologic group. Withdrawals from sandstone and carbonate-rock aquifers for public-supply (713 Mgal/d), irrigation (469 Mgal/d), and self-supplied domestic (253 Mgal/d) uses accounted for about 84 percent of the total withdrawals from this lithologic group. Although water was withdrawn from sandstone and carbonate-rock aquifers in 25 States, 65 percent of the total withdrawn was in Texas (651 Mgal/d), Pennsylvania (238 Mgal/d), and Florida (223 Mgal/d)

Maternal B vitamins: effects on offspring weight and DNA methylation at genomically imprinted domains

Abstract Background Inadequate maternal nutrition during early fetal development can create permanent alterations in the offspring, leading to poor health outcomes. While nutrients involved in one-carbon cycle metabolism are important to fetal growth, associations with specific nutrients remain inconsistent. This study estimates associations between maternal vitamins B12, B6 (pyridoxal phosphate [PLP] and 4-pyridoxic acid [PA]), and homocysteine (Hcy) concentrations, offspring weight (birth weight and 3-year weight gain), and DNA methylation at four differentially methylated regions (DMRs) known to be involved in fetal growth and development (H19, MEG3, SGCE/PEG10, and PLAGL1). Methods Study participants (n = 496) with biomarker and birth weight data were enrolled as part of the Newborn Epigenetics STudy. Weight gain data were available for 273 offspring. Among 484 mother-infant pairs, DNA methylation at regulatory sequences of genomically imprinted genes was measured in umbilical cord blood DNA using bisulfite pyrosequencing. We used generalized linear models to estimate associations. Results Multivariate adjusted regression models revealed an inverse association between maternal Hcy concentration and male birth weight (β = −210.40, standard error (SE) = 102.08, p = 0.04). The offspring of the mothers in the highest quartile of B12 experienced lower weight gain between birth and 3 years compared to the offspring of the mothers in the lowest (β = −2203.03, SE = 722.49, p = 0.003). Conversely, maternal PLP was associated with higher weight gain in males; higher maternal PLP concentrations were also associated with offspring DNA methylation levels at the MEG3 DMR (p < 0.01). Conclusions While maternal concentrations of B12, B6, and Hcy do not associate with birth weight overall, they may play an important role in 3-year weight gain. This is the first study to report an association between maternal PLP and methylation at the MEG3 DMR which may be an important epigenetic tag for maternal B vitamin adequacy

A stable isotope perspective on archaeological agricultural variability and Neolithic experimentation in India

Agriculture has been crucial in sustaining human populations in South Asia across dramatically variable environments for millennia. Until recently, however, the origins of this mode of subsistence in India have been discussed in terms of population migration and crop introduction, with limited focus on how agricultural packages were formulated and utilised in local contexts. Here, we report the first measurements of stable carbon and nitrogen isotope values in well-preserved charred crop remains from sites spanning the Neolithic/Chalcolithic to the Early Historic in two very different environmental zones: tropical East India and the semi-arid Deccan. The results show that this approach offers direct insight into prehistoric crop management under contrasting environmental constraints. Our preliminary results plausibly suggest that early farmers in India experimented with and made strategic use of water and manure resources in accordance with specific crop requirements and under varying environmental constraints. We suggest that the development of modern crop isotope baselines across India, and the application of this methodology to archaeological assemblages, has the potential to yield detailed insight into agroecology in India's past

An Automated Procedure to Identify Biomedical Articles that Contain Cancer-associated Gene Variants

The proliferation of biomedical literature makes it increasingly difficult for researchers to find and manage relevant information. However, identifying research articles containing mutation data, a requisite first step in integrating large and complex mutation data sets, is currently tedious, time-consuming and imprecise. More effective mechanisms for identifying articles containing mutation information would be beneficial both for the curation of mutation databases and for individual researchers. We developed an automated method that uses information extraction, classifier, and relevance ranking techniques to determine the likelihood of MEDLINE abstracts containing information regarding genomic variation data suitable for inclusion in mutation databases. We targeted the CDKN2A (p16) gene and the procedure for document identification currently used by CDKN2A Database curators as a measure of feasibility. A set of abstracts was manually identified from a MEDLINE search as potentially containing specific CDKN2A mutation events. A subset of these abstracts was used as a training set for a maximum entropy classifier to identify text features distinguishing relevant from not relevant abstracts. Each document was represented as a set of indicative word, word pair, and entity tagger-derived genomic variation features. When applied to a test set of 200 candidate abstracts, the classifier predicted 88 articles as being relevant; of these, 29 of 32 manuscripts in which manual curation found CDKN2A sequence variants were positively predicted. Thus, the set of potentially useful articles that a manual curator would have to review was reduced by 56%, maintaining 91% recall (sensitivity) and more than doubling precision (positive predictive value). Subsequent expansion of the training set to 494 articles yielded similar precision and recall rates, and comparison of the original and expanded trials demonstrated that the average precision improved with the larger data set. Our results show that automated systems can effectively identify article subsets relevant to a given task and may prove to be powerful tools for the broader research community. This procedure can be readily adapted to any or all genes, organisms, or sets of documents

High Sensitivity Array Observations of the z=1.87 Sub-Millimeter Galaxy GOODS 850-3

We present sensitive phase-referenced VLBI results on the radio continuum emission from the z=1.87 luminous submillimeter galaxy (SMG) GOODS 850-3. The observations were carried out at 1.4 GHz using the High Sensitivity Array (HSA). Our sensitive tapered VLBI image of GOODS 850-3 at 0.47 x 0.34 arcsec (3.9 x 2.9 kpc) resolution shows a marginally resolved continuum structure with a peak flux density of 148 \pm 38 uJy/beam, and a total flux density of 168 \pm 73 uJy, consistent with previous VLA and MERLIN measurements. The derived intrinsic brightness temperature is > 5 \pm 2 x 10^3 K. The radio continuum position of this galaxy coincides with a bright and extended near-infrared source that nearly disappears in the deep HST optical image, indicating a dusty source of nearly 9 kpc in diameter. No continuum emission is detected at the full VLBI resolution (13.2 x 7.2 mas, 111 x 61 pc), with a 4-sigma point source upper limit of 26 uJy/beam, or an upper limit to the intrinsic brightness temperature of 4.7 x 10^5 K. The extent of the observed continuum source at 1.4 GHz and the derived brightness temperature limits are consistent with the radio emission (and thus presumably the far-infrared emission) being powered by a major starburst in GOODS 850-3, with a star formation rate of ~2500 M_sun/yr. Moreover, the absence of any continuum emission at the full resolution of the VLBI observations indicates the lack of a compact radio AGN source in this z=1.87 SMG.Comment: 19 pages, 4 figures, accepted for publication in A

A 22-year Southern Sky Survey for Transient and Variable Radio Sources using the Molonglo Observatory Synthesis Telescope

We describe a 22-year survey for variable and transient radio sources, performed with archival images taken with the Molonglo Observatory Synthesis Telescope (MOST). This survey covers 2775 \unit{deg^2} of the sky south of $\delta < -30\degree$ at an observing frequency of 843 MHz, an angular resolution of 45 \times 45 \csc | \delta| \unit{arcsec^2} and a sensitivity of 5 \sigma \geq 14 \unit{mJy beam^{-1}}. We describe a technique to compensate for image gain error, along with statistical techniques to check and classify variability in a population of light curves, with applicability to any image-based radio variability survey. Among radio light curves for almost 30000 sources, we present 53 highly variable sources and 15 transient sources. Only 3 of the transient sources, and none of the variable sources have been previously identified as transient or variable. Many of our variable sources are suspected scintillating Active Galactic Nuclei. We have identified three variable sources and one transient source that are likely to be associated with star forming galaxies at $z \simeq 0.05$, but whose implied luminosity is higher than the most luminous known radio supernova (SN1979C) by an order of magnitude. We also find a class of variable and transient source with no optical counterparts.Comment: Accepted for publication in MNRAS. 34 pages, 30 figures, 7 table

Patient/Family Education for Newly Diagnosed Pediatric Oncology Patients

There is a paucity of data to support evidence-based practices in the provision of patient/family education in the context of a new childhood cancer diagnosis. Since the majority of children with cancer are treated on pediatric oncology clinical trials, lack of effective patient/family education has the potential to negatively affect both patient and clinical trial outcomes. The Children’s Oncology Group Nursing Discipline convened an interprofessional expert panel from within and beyond pediatric oncology to review available and emerging evidence and develop expert consensus recommendations regarding harmonization of patient/family education practices for newly diagnosed pediatric oncology patients across institutions. Five broad principles, with associated recommendations, were identified by the panel, including recognition that (1) in pediatric oncology, patient/family education is family-centered; (2) a diagnosis of childhood cancer is overwhelming and the family needs time to process the diagnosis and develop a plan for managing ongoing life demands before they can successfully learn to care for the child; (3) patient/family education should be an interprofessional endeavor with 3 key areas of focus: (a) diagnosis/treatment, (b) psychosocial coping, and (c) care of the child; (4) patient/family education should occur across the continuum of care; and (5) a supportive environment is necessary to optimize learning. Dissemination and implementation of these recommendations will set the stage for future studies that aim to develop evidence to inform best practices, and ultimately to establish the standard of care for effective patient/family education in pediatric oncology

Baseline representativeness of patients in clinics enrolled in the PRimary care Opioid Use Disorders treatment (PROUD) trial: comparison of trial and non-trial clinics in the same health systems

BACKGROUND: Pragmatic primary care trials aim to test interventions in real world health care settings, but clinics willing and able to participate in trials may not be representative of typical clinics. This analysis compared patients in participating and non-participating clinics from the same health systems at baseline in the PRimary care Opioid Use Disorders treatment (PROUD) trial. METHODS: This observational analysis relied on secondary electronic health record and administrative claims data in 5 of 6 health systems in the PROUD trial. The sample included patients 16-90 years at an eligible primary care visit in the 3 years before randomization. Each system contributed 2 randomized PROUD trial clinics and 4 similarly sized non-trial clinics. We summarized patient characteristics in trial and non-trial clinics in the 2 years before randomization ( baseline ). Using mixed-effect regression models, we compared trial and non-trial clinics on a baseline measure of the primary trial outcome (clinic-level patient-years of opioid use disorder (OUD) treatment, scaled per 10,000 primary care patients seen) and a baseline measure of the secondary trial outcome (patient-level days of acute care utilization among patients with OUD). RESULTS: Patients were generally similar between the 10 trial clinics (n = 248,436) and 20 non-trial clinics (n = 341,130), although trial clinics\u27 patients were slightly younger, more likely to be Hispanic/Latinx, less likely to be white, more likely to have Medicaid/subsidized insurance, and lived in less wealthy neighborhoods. Baseline outcomes did not differ between trial and non-trial clinics: trial clinics had 1.0 more patient-year of OUD treatment per 10,000 patients (95% CI: - 2.9, 5.0) and a 4% higher rate of days of acute care utilization than non-trial clinics (rate ratio: 1.04; 95% CI: 0.76, 1.42). CONCLUSIONS: trial clinics and non-trial clinics were similar regarding most measured patient characteristics, and no differences were observed in baseline measures of trial primary and secondary outcomes. These findings suggest trial clinics were representative of comparably sized clinics within the same health systems. Although results do not reflect generalizability more broadly, this study illustrates an approach to assess representativeness of clinics in future pragmatic primary care trials

Paternal obesity is associated with IGF2 hypomethylation in newborns: results from a Newborn Epigenetics Study (NEST) cohort

Data from epidemiological and animal model studies suggest that nutrition during pregnancy may affect the health status of subsequent generations. These transgenerational effects are now being explained by disruptions at the level of the epigenetic machinery. Besides in vitro environmental exposures, the possible impact on the reprogramming of methylation profiles at imprinted genes at a much earlier time point, such as during spermatogenesis or oogenesis, has not previously been considered. In this study, our aim was to determine associations between preconceptional obesity and DNA methylation profiles in the offspring, particularly at the differentially methylated regions (DMRs) of the imprinted Insulin-like Growth Factor 2 (IGF2) gene

No excess of mitochondrial DNA deletions within muscle in progressive multiple sclerosis

BACKGROUND: Mitochondrial dysfunction is an established feature of multiple sclerosis (MS). We recently described high levels of mitochondrial DNA (mtDNA) deletions within respiratory enzyme-deficient (lacking mitochondrial respiratory chain complex IV with intact complex II) neurons and choroid plexus epithelial cells in progressive MS. OBJECTIVES: The objective of this paper is to determine whether respiratory enzyme deficiency and mtDNA deletions in MS were in excess of age-related changes within muscle, which, like neurons, are post-mitotic cells that frequently harbour mtDNA deletions with ageing and in disease. METHODS: In progressive MS cases (n=17), known to harbour an excess of mtDNA deletions in the central nervous system (CNS), and controls (n=15), we studied muscle (paraspinal) and explored mitochondria in single fibres. Histochemistry, immunohistochemistry, laser microdissection, real-time polymerase chain reaction (PCR), long-range PCR and sequencing were used to resolve the single muscle fibres. RESULTS: The percentage of respiratory enzyme-deficient muscle fibres, mtDNA deletion level and percentage of muscle fibres harbouring high levels of mtDNA deletions were not significantly different in MS compared with controls. CONCLUSION: Our findings do not provide support to the existence of a diffuse mitochondrial abnormality involving multiple systems in MS. Understanding the cause(s) of the CNS mitochondrial dysfunction in progressive MS remains a research priority