Effects of Declining Senses Nutrients, Functions and Nutrient Classes Nutrients in Body Composition Water Nutrient Utilization
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Mineral Classifications-No Links
CLASSIFYING MINERALS Minerals are divided into nine (9) broad classifications. They are typically classified based on the negatively charged (anionic) portion of their chemical composition. For example, copper oxide (CuO) consists of copper (Cu ++ ) and oxygen (O -- ) ions, and the negatively charged oxygen ion puts it in the “Oxide” classification (which also includes iron oxide, titanium dioxide, etc). The classifications are: Silicate class The largest group of minerals by far, the silicates are mostly composed of silicon and oxygen, combined with ions like aluminum, magnesium, iron, and calcium. Some important rock-forming silicates include the feldspars, quartz, olivines, pyroxenes, garnets, and micas. Carbonate class 2− The carbonate minerals contain the anion (CO 3) . They are deposited in marine settings from accumulated shells of marine life and also in evaporitic areas like the Great Salt Lake and karst regions where they form caves, stalactites and stalagmites. Typical carbonates include calcite and aragonite (both calcium carbonate), dolomite (magnesium/calcium carbonate) and siderite (iron carbonate). The carbonate class also includes the nitrate and borate minerals. Sulfate class 2− Sulfate minerals all contain the sulfate anion, SO 4 . Sulfates commonly form in evaporitic settings where highly saline waters slowly evaporate, in hydrothermal vein systems as gangue minerals and as secondary oxidation products of original sulfide minerals. Common sulfates include anhydrite (calcium sulfate), celestine (strontium sulfate), barite (barium sulfate), and gypsum (hydrated calcium sulfate). The sulfate class also includes the chromate, molybdate, selenate, sulfite, tellurate, and tungstate minerals. Halide class The halide minerals form the natural salts and include fluorite (calcium fluoride), halite (sodium chloride) and sylvite (potassium chloride). -
Karpatite C24H12 C 2001-2005 Mineral Data Publishing, Version 1
Karpatite C24H12 c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Monoclinic. Point Group: 2/m. Crystals are acicular, thin tabular parallel to [001], showing {001}, {100}, {201}, many other forms, to 1 cm; typically in bladed groups and fibrous radiating aggregates. Physical Properties: Cleavage: On {001}, {100}, {201}, perfect. Fracture: Splintery. Tenacity: Flexible, nearly plastic. Hardness = ∼1 D(meas.) = 1.35–1.40 D(calc.) = 1.29–1.42 Flammable; fluoresces sky-blue under LW and SW UV. Optical Properties: Subtranslucent. Color: Yellow, yellowish brown on exposure. Luster: Vitreous. Optical Class: Biaxial (–) or (+). Orientation: X = b; Z ∧ c =21◦. Dispersion: rv, extreme. α = 1.780(2) β = 1.977–1.982 γ = 2.05–2.15 2V(meas.) = 96◦–115◦ Cell Data: Space Group: P 21/c or P 2/c (synthetic). a = 10.035 b = 4.695 c = 16.014 β = 112◦ Z=2 X-ray Powder Pattern: Olenevo, Ukraine. 9.40 (10), 3.52 (9), 7.52 (8), 3.97 (7), 3.05 (6), 7.25 (5), 3.43 (4) Chemistry: (1) (2) C 96.04 95.97 H 4.04 4.03 O Total 100.08 100.00 (1) Olenevo, Ukraine. (2) C24H12 (coronene). Occurrence: In cavities at the contact of diorite porphyry with argillites (Olenevo, Ukraine); a low-temperature hydrothermal mineral (California, USA). Association: Idrialite, amorphous organic material, calcite, barite, quartz, cinnabar, metacinnabar (Olenevo, Ukraine); cinnabar, quartz (California, USA). Distribution: From near Olenevo, Transcarpathian region, western Ukraine. At Tamvotney, Kamchatka Peninsula, Russia. From the Picacho mercury mine, south of New Idria, San Benito Co., California, USA. -
A Computational Approach for Identifying Plant-Based Foods for Addressing Vitamin Deficiency Diseases
University of Vermont ScholarWorks @ UVM UVM Honors College Senior Theses Undergraduate Theses 2015 A Computational Approach for Identifying Plant-Based Foods for Addressing Vitamin Deficiency Diseases Christina Yu University of Vermont Indra Neil Sarkar University of Vermont Follow this and additional works at: https://scholarworks.uvm.edu/hcoltheses Recommended Citation Yu, Christina and Sarkar, Indra Neil, "A Computational Approach for Identifying Plant-Based Foods for Addressing Vitamin Deficiency Diseases" (2015). UVM Honors College Senior Theses. 212. https://scholarworks.uvm.edu/hcoltheses/212 This Honors College Thesis is brought to you for free and open access by the Undergraduate Theses at ScholarWorks @ UVM. It has been accepted for inclusion in UVM Honors College Senior Theses by an authorized administrator of ScholarWorks @ UVM. For more information, please contact [email protected]. A Computational Approach for Identifying Plant-Based Foods for Addressing Vitamin Deficiency Diseases Christina Yu1 and Indra Neil Sarkar2,3 Key words: computing methodologies, vitamin deficiency diseases, vegetarian diet 1 Undergraduate Program in Biochemistry, University of Vermont, Burlington, VT 2 Department of Microbiology and Molecular Genetics, University of Vermont, Burlington, VT 3 Center for Clinical and Translational Science, University of Vermont, Burlington, VT 1 ABSTRACT Vitamins are nutrients that are essential to human health, and deficiencies have been shown to cause severe diseases. In this study, a computational approach was used to identify vitamin deficiency diseases and plant-based foods with vitamin content. Data from the United States Department of Agriculture Standard Reference (SR27), National Library of Medicine's Medical Subject Headings and MEDLINE, and Wikipedia were combined to identify vitamin deficiency diseases and vitamin content of plant-based foods. -
VITAMINS by Dr
VITAMINS BY Dr. Samy Ali Hussein Aziza Professor of Biochemistry and Clinical Biochemistry Faculty of Veterinary Medicine, Moshtohor, Benha University, Egypt. E-Mail: [email protected] Vitamins Vitamins are organic compounds characterized by: Essential for normal health and growth. Essential for biological activity in the body. Present in food in very small concentration. Not enter in the tissue structure as carbohydrates, lipids and proteins. Act as catalysts and are not oxidized to give energy as carbohydrates, lipids and proteins. Deficiency of any vitamin in the body results in production of specific diseases. Many vitamin function as coenzymes. Not synthesized in the body by anabolic reaction, therefore should be taken in the diet. Some vitamin are present in food in the form of provitamins. Provitamin They are vitamin precursors. Example: • Carotenes are provitamin A. • 7- dehydrocholesterol are provitamin D3 Vitamer When a vitamin is present in more than one chemical formula each is called a vitamers Example: • Vitamin A has Two vitamers A1 and A2. • Vitamin D has two vitamers D2 and D3. • Vitamin E has four vitamers alpha, beta, gama, delta. Vitagen These include both essential Amino acids and essential fatty acids. Classification of vitamins Vitamins can be classified according to their solubility and their function in metabolism into: I- Fat soluble vitamins II- Water soluble vitamins I- Fat Soluble Vitamins Vitamin A Vitamin D Vitamin E Vitamin K II-WATER SOLUBLE VITAMINS I- B- complex – Thiamine (B1) – Riboflavin (B2) – Niacin (B3) – Folic acid – Pyridoxine (B6) – Vitamin B12 – Pantothenic Acid – Biotin II- Non B- complex : Vitamin C (ascorbic acid). B- complex a- Energy-releasing. -
Flavin Adenine Dinucleotide Status and the Effects of High-Dose Riboflavin Treatment in Short-Chain Acyl-Coa Dehydrogenase Deficiency
0031-3998/10/6703-0304 Vol. 67, No. 3, 2010 PEDIATRIC RESEARCH Printed in U.S.A. Copyright © 2010 International Pediatric Research Foundation, Inc. Flavin Adenine Dinucleotide Status and the Effects of High-Dose Riboflavin Treatment in Short-Chain Acyl-CoA Dehydrogenase Deficiency BIANCA T. VAN MALDEGEM, MARINUS DURAN, RONALD J. A. WANDERS, HANS R. WATERHAM, AND FRITS A. WIJBURG Department of Pediatrics [B.T.M, F.A.W.] and Laboratory Genetic Metabolic Diseases [M.D., R.J.A.W., H.R.W.], University of Amsterdam, 1105 AZ Amsterdam, the Netherlands ABSTRACT: Short-chain acyl-CoA dehydrogenase deficiency most US states (15). In addition, potential treatment options (SCADD) is an inborn error, biochemically characterized by in- for SCADD have never been systematically studied. creased plasma butyrylcarnitine (C4-C) concentration and increased SCADD is caused by decreased activity of the first enzyme ethylmalonic acid (EMA) excretion and caused by rare mutations of the short-chain fatty acid -oxidation spiral, which cata- and/or common gene variants in the SCAD encoding gene. Although lyzes the dehydrogenation of butyryl-CoA (C4-CoA). When its clinical relevance is not clear, SCADD is included in most US SCAD activity is impaired, C4-CoA will accumulate and is newborn screening programs. Riboflavin, the precursor of flavin subsequently converted into different metabolites including 1) adenine dinucleotide (FAD, cofactor), might be effective for treating the corresponding carnitine-ester, i.e. butyrylcarnitine (C4-C); SCADD. We assessed the FAD status and evaluated the effects of riboflavin treatment in a prospective open-label cohort study involv- 2) the corresponding glycine ester (butyrylglycine); 3) bu- ing 16 patients with SCADD, subdivided into mutation/mutation tyrate; and 4) ethylmalonic acid (EMA). -
Carbon Mineral Ecology: Predicting the Undiscovered Minerals of Carbon
American Mineralogist, Volume 101, pages 889–906, 2016 Carbon mineral ecology: Predicting the undiscovered minerals of carbon ROBERT M. HAZEN1,*, DANIEL R. HUMMER1, GRETHE HYSTAD2, ROBERT T. DOWNS3, AND JOSHUA J. GOLDEN3 1Geophysical Laboratory, Carnegie Institution, 5251 Broad Branch Road NW, Washington, D.C. 20015, U.S.A. 2Department of Mathematics, Computer Science, and Statistics, Purdue University Calumet, Hammond, Indiana 46323, U.S.A. 3Department of Geosciences, University of Arizona, 1040 East 4th Street, Tucson, Arizona 85721-0077, U.S.A. ABSTRACT Studies in mineral ecology exploit mineralogical databases to document diversity-distribution rela- tionships of minerals—relationships that are integral to characterizing “Earth-like” planets. As carbon is the most crucial element to life on Earth, as well as one of the defining constituents of a planet’s near-surface mineralogy, we focus here on the diversity and distribution of carbon-bearing minerals. We applied a Large Number of Rare Events (LNRE) model to the 403 known minerals of carbon, using 82 922 mineral species/locality data tabulated in http://mindat.org (as of 1 January 2015). We find that all carbon-bearing minerals, as well as subsets containing C with O, H, Ca, or Na, conform to LNRE distributions. Our model predicts that at least 548 C minerals exist on Earth today, indicating that at least 145 carbon-bearing mineral species have yet to be discovered. Furthermore, by analyzing subsets of the most common additional elements in carbon-bearing minerals (i.e., 378 C + O species; 282 C + H species; 133 C + Ca species; and 100 C + Na species), we predict that approximately 129 of these missing carbon minerals contain oxygen, 118 contain hydrogen, 52 contain calcium, and more than 60 contain sodium. -
Nanostructural Origin of Blue Fluorescence in the Mineral Karpatite
Potticary, J. , Jensen, T. T., & Hall, S. R. (2017). Nanostructural origin of blue fluorescence in the mineral karpatite. Scientific Reports, 7(1), [9867]. https://doi.org/10.1038/s41598-017-10261-w Publisher's PDF, also known as Version of record License (if available): CC BY Link to published version (if available): 10.1038/s41598-017-10261-w Link to publication record in Explore Bristol Research PDF-document This is the final published version of the article (version of record). It first appeared online via Nature at https://www.nature.com/articles/s41598-017-10261-w. Please refer to any applicable terms of use of the publisher. University of Bristol - Explore Bristol Research General rights This document is made available in accordance with publisher policies. Please cite only the published version using the reference above. Full terms of use are available: http://www.bristol.ac.uk/red/research-policy/pure/user-guides/ebr-terms/ www.nature.com/scientificreports OPEN Nanostructural origin of blue fuorescence in the mineral karpatite Received: 9 June 2017 Jason Potticary 1,2, Torsten T. Jensen 1,3 & Simon R. Hall1 Accepted: 7 August 2017 The colour of crystals is a function of their atomic structure. In the case of organic crystals, it is the Published: xx xx xxxx spatial relationships between molecules that determine the colour, so the same molecules in the same arrangement should produce crystals of the same colour, regardless of whether they arise geologically or synthetically. There is a naturally-occurring organic crystal known as karpatite which is prized for its beautiful blue fuorescence under ultra-violet illumination. -
Challenges to Quantify Total Vitamin Activity: How to Combine the Contribution of Diverse Vitamers?
REVIEW CURRENT DEVELOPMENTS IN NUTRITION Challenges to Quantify Total Vitamin Activity: How to Combine the Contribution of Diverse Vitamers? Jette Jakobsen ,1 Alida Melse-Boonstra ,2 and Michael Rychlik 3,4 1National Food Institute, Technical University of Denmark, Kongens Lyngby, Denmark; 2Division of Human Nutrition and Health, Wageningen University & Research, Wageningen, the Netherlands; 3Technical University of Munich, Freising, Germany; and 4Centre for Nutrition and Food Sciences, Queensland Alliance for Agriculture and Food Innovation, The University of Queensland, Coopers Plains, Australia ABSTRACT This state-of-the-art review aims to highlight the challenges in quantifying vitamin activity in foods that contain several vitamers of a group, using as examples the fat-soluble vitamins A and D as well as the water-soluble folate. The absorption, metabolism, and physiology of these examples are described along with the current analytical methodology, with an emphasis on approaches to standardization. Moreover, the major food sources for the vitamins are numerated. The article focuses particularly on outlining the so-called SLAMENGHI factors influencing a vitamer’s’ ability to act as a vitamin, that is, molecular species, linkage, amount, matrix, effectors of absorption, nutrition status, genetics, host-related factors, and the interaction of these. After summarizing the current approaches to estimating the total content of each vitamin group, the review concludes by outlining the research gaps and future perspectives in vitamin analysis. There are no standardized methods for the quantification of the vitamers of vitamin A, vitamin D, and folate in foods. For folate and β-carotene, a difference in vitamer activity between foods and supplements has been confirmed, whereas no difference has been observed for vitamin D. -
Department of Statistics Academic Program Review Spring 2015
Department of Statistics Academic Program Review Spring 2015 Department of Statistics • Texas A&M University • 3143 TAMU • College Station, TX 77843-3143 (979) 845-3141 • www.stat.tamu.edu Table of Contents I. Introduction Brief History of the Department……………………………………………………. 4 Mission and Goals………………………………………………………………….. 8 Administrative Structure of the Department………………………………………... 11 Resources…………………………………………………………………………... 13 Analysis……………………………………………………………………………. 14 Undergraduate Program……………………………………………………………. 15 Graduate Program………………………………………………………………….. 16 Professional Education……………………………………………………………... 19 Challenges and Opportunities……………………………………………………… 20 Assessment………………………………………………………………………… 22 II. Student Report Graduate Program in Statistics……………………………………………………… 28 Master of Science Program…………………………………………………………. 29 Doctor of Philosophy Program……………………………………………………... 32 Internship Program…………………………………………………………………. 35 Undergraduate Course Offerings…………………………………………………… 36 Graduate Course Offerings………………………………………………………… 37 Scheduling Coursework…………………………………………………………….. 42 Graduate Program Admissions Criteria……………………………………………... 43 GRE Scores for First Time Students………………………………………………... 44 Graduate Students Applied, Admitted, and Enrolled ………………………………. 45 Students by GPR Range……………………………………………………………. 48 Institutional Support for Full Time Students……………………………………….. 50 Honors & Awards Received by Students…………………………………………… 51 Statistics Graduate Student Association…………………………………………….. 54 Student Publications……………………………………………………………….. -
Comprehensive Vitamer Profiling of Folate Mono
H OH metabolites OH Article Comprehensive Vitamer Profiling of Folate Mono- and Polyglutamates in Baker’s Yeast (Saccharomyces cerevisiae) as a Function of Different Sample Preparation Procedures Lena Gmelch 1, Daniela Wirtz 1, Michael Witting 1,2 , Nadine Weber 1 , Lisa Striegel 1 , Philippe Schmitt-Kopplin 1,2,* and Michael Rychlik 1,2,* 1 Chair of Analytical Food Chemistry, Technical University of Munich, 85354 Freising-Weihenstephan, Germany; [email protected] (L.G.); [email protected] (D.W.); [email protected] (M.W.); [email protected] (N.W.); [email protected] (L.S.) 2 Research Unit BioGeoChemistry, Helmholtz Zentrum Munich, 85764 Neuherberg, Germany * Correspondence: [email protected] (P.S.-K.); [email protected] (M.R.) Received: 14 June 2020; Accepted: 16 July 2020; Published: 23 July 2020 Abstract: Folates are a group of B9 vitamins playing an important role in many metabolic processes such as methylation reactions, nucleotide synthesis or oxidation and reduction processes. However, humans are not able to synthesize folates de novo and thus rely on external sources thereof. Baker’s yeast (Saccharomyces cerevisiae) has been shown to produce high amounts of this vitamin but extensive identification of its folate metabolism is still lacking. Therefore, we optimized and compared different sample preparation and purification procedures applying solid phase extraction (SPE). Strong anion exchange (SAX), C18 and hydrophilic–lipophilic-balanced (HLB) materials were tested for their applicability in future metabolomics studies. SAX turned out to be the preferred material for the quantitative purification of folates. Qualification of several folate vitamers was achieved by ultra-high pressure liquid chromatography quadrupole time of flight mass spectrometry (UHPLC-Q-ToF-MS) measurements and quantification was performed by liquid chromatography tandem mass spectrometry (LC-MS/MS) applying stable isotope dilution assays (SIDAs). -
Design Rules for Discovering 2D Materials from 3D Crystals
Design Rules for Discovering 2D Materials from 3D Crystals by Eleanor Lyons Brightbill Collaborators: Tyler W. Farnsworth, Adam H. Woomer, Patrick C. O'Brien, Kaci L. Kuntz Senior Honors Thesis Chemistry University of North Carolina at Chapel Hill April 7th, 2016 Approved: ___________________________ Dr Scott Warren, Thesis Advisor Dr Wei You, Reader Dr. Todd Austell, Reader Abstract Two-dimensional (2D) materials are championed as potential components for novel technologies due to the extreme change in properties that often accompanies a transition from the bulk to a quantum-confined state. While the incredible properties of existing 2D materials have been investigated for numerous applications, the current library of stable 2D materials is limited to a relatively small number of material systems, and attempts to identify novel 2D materials have found only a small subset of potential 2D material precursors. Here I present a rigorous, yet simple, set of criteria to identify 3D crystals that may be exfoliated into stable 2D sheets and apply these criteria to a database of naturally occurring layered minerals. These design rules harness two fundamental properties of crystals—Mohs hardness and melting point—to enable a rapid and effective approach to identify candidates for exfoliation. It is shown that, in layered systems, Mohs hardness is a predictor of inter-layer (out-of-plane) bond strength while melting point is a measure of intra-layer (in-plane) bond strength. This concept is demonstrated by using liquid exfoliation to produce novel 2D materials from layered minerals that have a Mohs hardness less than 3, with relative success of exfoliation (such as yield and flake size) dependent on melting point. -
By Michael Fleischer and Constance M. Schafer Open-File Report 81
U.S. DEPARTMENT OF THE INTERIOR GEOLOGICAL SURVEY THE FORD-FLEISCHER FILE OF MINERALOGICAL REFERENCES, 1978-1980 INCLUSIVE by Michael Fleischer and Constance M. Schafer Open-File Report 81-1174 This report is preliminary and has not been reviewed for conformity with U.S. Geological Survey editorial standards 1981 The Ford-Fleischer File of Mineralogical References 1978-1980 Inclusive by Michael Fleischer and Constance M. Schafer In 1916, Prof. W.E. Ford of Yale University, having just published the third Appendix to Dana's System of Mineralogy, 6th Edition, began to plan for the 7th Edition. He decided to create a file, with a separate folder for each mineral (or for each mineral group) into which he would place a citation to any paper that seemed to contain data that should be considered in the revision of the 6th Edition. He maintained the file in duplicate, with one copy going to Harvard University, when it was agreed in the early 1930's that Palache, Berman, and Fronde! there would have the main burden of the revision. A number of assistants were hired for the project, including C.W. Wolfe and M.A. Peacock to gather crystallographic data at Harvard, and Michael Fleischer to collect and evaluate chemical data at Yale. After Prof. Ford's death in March 1939, the second set of his files came to the U.S. Geological Survey and the literature has been covered since then by Michael Fleischer. Copies are now at the U.S. Geological Survey at Reston, Va., Denver, Colo., and Menlo Park, Cal., and at the U.S.