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  • 1
    Online Resource
    Online Resource
    San Diego :Elsevier Science & Technology,
    Keywords: Vitamin D. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (2190 pages)
    Edition: 3rd ed.
    ISBN: 9780123819796
    DDC: 612.399
    Language: English
    Note: e9780123819789v1.pdf -- Front Cover -- Vitamin D -- Copyright -- Contents -- Preface to the 3rd Edition -- Preface to the 2nd Edition -- Preface to the 1st Edition -- Contributors -- Introduction -- Abbreviations -- Relevant Lab Values in Adults and Children -- Criteria for Vitamin D Deficiency: 25(OH)D Serum Levels -- Approximate normal ranges for serum values in adultsaaNormal ranges differ in various laboratories and these values are pro ... -- Approximate normal ranges for serum values in childrena -- Useful equivalencies of different units -- Section I -Chemistry, Metabolism, Circulation -- Chapter 1 - Historical Overview of Vitamin D -- Discovery of the Vitamins -- Discovery that Vitamin D is not a Vitamin -- Isolation and Identification of Nutritional Forms of Vitamin D -- Discovery of the Physiological Functions of Vitamin D -- Discovery of the Hormonal Form of Vitamin D -- Acknowledgments -- References -- Chapter 2 - Photobiology of Vitamin D -- Introduction -- Historical Perspective -- Photobiology of Vitamin D -- Role of Sunlight and Dietary Vitamin D in Bone Health, Overall Health, and Well-Being -- Sunlight, Vitamin D, and Skin Cancer -- Conclusion -- Acknowledgment -- References -- Chapter 3 - The Activating Enzymes of Vitamin D Metabolism (25- and 1α-Hydroxylases) -- Introduction -- General Information Regarding Vitamin D Hydroxylases -- Vitamin D3-25-Hydroxylases -- 25-Hydroxyvitamin D-1α-Hydroxylase -- Additional Topics -- References -- Chapter 4 - CYP24A1: Structure, Function, and Physiological Role -- Overview -- CYP24A1-Catalyzed Pathways -- Structure-Function Relationships -- Putative CYP24A1 Involvement in Nonclassical Systems -- Perspectives -- References -- Chapter 5 - The Vitamin D Binding Protein DBP -- Introduction -- Vitamin D Binding Protein: Protein and Gene Structure -- Functions of DBP. , Conclusions and Perspectives -- References -- Chapter 6 - Industrial Aspects of Vitamin D -- History of Vitamin D Leading To Commercialization -- Manufacture of the Provitamins -- Irradiation of 7-Dehydrocholesterol and Ergosterol -- Metabolite Manufacture -- Analytical -- Dietary Requirements -- Economic Aspects -- Storage and Shipping -- References -- Section II -Mechanisms of Action -- Chapter 7 - The Vitamin D Receptor: Biochemical, Molecular, Biological, and Genomic Era Investigations -- Introduction -- Vitamin D Biology -- Discovery of the Vitamin D Receptor -- VDR Research: The Biochemical Era -- VDR Research: The Molecular Biological Era -- VDR Research: The Genomic Era -- VDR Chromosomal Gene: Structure and Molecular Regulation -- Concluding Comments -- Acknowledgment -- References -- Chapter 8 - Nuclear Vitamin D Receptor: Natural Ligands, Molecular Structure-Function, and Transcriptional Control of Vital ... -- Ligands, Gene Targets, and Biological Actions of Vdr -- VDR as a Member of the Nuclear Receptor Superfamily -- Molecular Structure-Function Of VDR -- Mechanisms of VDR-Mediated Control of Gene Expression -- VDR-Mediated Control of Vital Genes in Healthful Aging and Disease Prevention -- Conclusions and Perspectives -- Acknowledgment -- References -- Chapter 9 - Structural Basis for Ligand Activity in VDR -- Introduction -- Crystal Structure of hvdrΔ Bound to 1,25(Oh)2d3 -- Crystal Structure of zVDR Wild-Type LBD Bound to 1,25(OH)2D3 -- Structure of VDR LBD Complexed to Superagonist Ligands -- Structures of VDR Complexed to 2α-Substituted Analogs -- Structures of VDR With Nonsteroidal Ligands -- Structures of VDR With Analogs that Induce Structural Rearrangements -- Structural Basis for Vitamin D Receptor Antagonism -- Structure-based Design of Novel Superagonist Analogs -- Conclusion -- References. , Chapter 10 - Coregulators of VDR-mediated Gene Expression -- Introduction -- Coactivators of VDR -- Corepressors -- Conclusion - Integrated Model of Coregulator Activity -- References -- Chapter 11 - Target Genes of Vitamin D: Spatio-temporal Interaction of Chromatin, VDR, and Response Elements -- Introduction -- Transcriptional Regulation by 1,25(OH)2D3 -- Genomic VDR-Binding sites -- VDR Target Genes -- VDR Target Gene Analysis -- Transcriptional Cycling -- Conclusion -- Acknowledgments -- References -- Chapter 12 - Epigenetic Modifications in Vitamin D Receptor-mediated Transrepression -- Introduction -- WINAC: A Novel VDR-Associating ATP-Dependent Chromatin Remodeling Complex -- E-Box Motif Negative VDRE Mediates 1,25(OH)2D3-Induced Transrepression -- Coregulator Switching at E-Box nVdres in Ligand-Dependent Transrepression by VDR -- WINAC Mediates Ligand-Induced Transrepression by VDR -- 1,25(OH)2D3-Dependent VDR Transrepression Involves CpG Site Methylation in the CYP27B1 Promoter -- Cell-Cycle-Independent DNA Demethylation During CYP27B1 Transcriptional Derepression -- MBD4 Mediates Active DNA Demethylation -- MBD4 is a Downstream Mediator in PTH Signaling-Induced Transcriptional Derepression -- Conclusion -- References -- Chapter 13 - Vitamin D and Wnt/β-Catenin Signaling -- Introduction -- WNT Signaling -- Antagonism of Wnt/β-Catenin Pathway by 1,25(OH)2D3 in Colon Cancer -- Wnt and 1,25(OH)2D3 in the Bone -- Wnt and 1,25(OH)2D3 in the Skin -- Conclusions -- References -- Chapter 14 - Vitamin D Response Element-binding Protein -- Introduction -- Current View of Steroid/Sterol Hormone Action -- New World Primates -- New World Primate-Like VItamin D Resistance in Man -- Heterogeneous Nuclear Ribonucleoproteins (hnRNPs) -- hnRNPs as Multi-Level, Multi-Site, cis-Binding Regulators of Gene Expression. , The Estrogen Response Element Binding Protein (ERE-BP) and the Intracellular Estrogen Binding Protein (IEBP) -- Compensation for the Dominant-Negative Acting, Response Element-Binding Proteins -- Conclusion -- References -- Chapter 15 - Vitamin D Sterol/VDR Conformational Dynamics and Nongenomic Actions -- 1α,25(OH)2-Vitamin D3 (1,25(OH)2D3) Regulation of Genomic Versus Nongenomic Signaling -- Vitamin D3 Sterol (VDS) Chemistry -- 1,25(OH)2D3 Mediated Rapid, Nongenomic Responses -- The Plasma Membrane Vitamin D Receptor -- The VDR Conformational Ensemble Model -- VDR Ligand Specificity: Does an Unliganded VDR Ever Exist in Vivo? -- References -- Section III -Mineral and Bone Homeostasis -- Chapter 16 - Genetic and Epigenetic Control of the Regulatory Machinery for Skeletal Development and Bone Formation: Contrib ... -- Programs of Bone Formation -- Nuclear Organization of the Regulatory Machinery for Bone Formation -- Epigenetic Mechanism for Lineage Commitment -- Gene Expression within the Three-Dimensional Context of Nuclear Architecture -- Chromatin Remodeling Facilitates Bone-Specific and Vitamin-D-Mediated Promoter Accessibility and Integration of Regulatory ... -- Scaffolding of Regulatory Components for Combinatorial Control of Gene Expression -- Closing Remarks -- Acknowledgments -- References -- Chapter 17 - Vitamin D Regulation of Osteoblast Function -- Introduction -- Properties of Mature Osteoblasts and Osteocytes -- Major Regulatory Functions of Osteoblasts and Osteocytes and Control by the Vitamin D Endocrine System -- Effects of 1,25(OH)2D3 on Osteoblast Differentiation -- Regulation of Intracellular Signaling Pathways by 1,25(OH)2D3 -- Summary and Conclusions -- Acknowledgments -- References -- Chapter 18 - Osteoclasts -- Introduction -- References. , Chapter 19 - Molecular Mechanisms for Regulation of Intestinal Calcium and Phosphate Absorption by Vitamin D -- An Overview of Intestinal Calcium Absorption -- Critical Role of VDR in Control of Intestinal Ca Absorption -- Can High Vitamin D Status Increase Intestinal Calcium Absorption? -- An Overview of Intestinal Phosphate Absorption -- Acknowledgments -- References -- Chapter 20 - The Calbindins: Calbindin-D28K and Calbindin-D9K and the Epithelial Calcium Channels TRPV5 and TRPV6 -- Introduction and General Considerations, The Calbindins -- Localization and Proposed Functional Significance of the Calbindins -- Regulation of Calbindin Gene Expression -- Epithelial Calcium Channels -- Conclusion -- References -- Chapter 21 - Mineralization -- Introduction -- Conclusions -- References -- Chapter 22 - Vitamin D Regulation of Type I Collagen Expression in Bone -- Introduction -- Regulation of Bone Collagen Synthesis -- Molecular Mechanisms of Regulation -- Conclusions and Perspectives -- References -- Chapter 23 - Target Genes: Bone Proteins -- Vitamin D and Skeletal Homeostasis -- Exogenous and Endogenous Sources of 1,25(OH)2D3 -- Direct Actions of Vitamin D in Bone -- Concluding Remarks -- References -- Chapter 24 - Vitamin D and the Calcium-Sensing Receptor -- Introduction -- What is the CaSR? -- Overview of Roles of CaSR and VDR in Maintaining Ca2+O Homeostasis -- The CaSR and VDR in Tissues Participating in Ca2+O Homeostasis -- The CaSR and VDR in Tissues Uninvolved in Ca2+O Homeostasis -- Polymorphisms of the CaSR and VDR and Calcium and Bone Homeostasis -- Summary and Perspectives -- References -- Chapter 25 - Effects of 1,25-Dihydroxyvitamin D3 on Voltage-Sensitive Calcium Channels in Osteoblast Differentiation and Mor ... -- Systemic and Intracellular Ca2+ Homeostasis -- Voltage-Sensitive Calcium Channels. , 1,25-Dihydroxyvitamin D3 Actions on Voltage-Sensitive Ca2+ Channels.
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  • 2
    Online Resource
    Online Resource
    San Diego :Elsevier Science & Technology,
    Keywords: Vitamin D. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (1970 pages)
    Edition: 2nd ed.
    ISBN: 9780080543642
    DDC: 612.399
    Language: English
    Note: 9780122526879v1 -- Front Cover -- Vitamin D -- Copyright Page -- Contents -- List of Contributors -- Preface to the 2nd Edition -- Preface to the 1st Edition -- Abbreviations -- Introduction -- Chapter 1. Historical Perspective -- Section I: CHEMISTRY, METABOLISM, AND CIRCULATION -- Chapter 2. Vitamin D Metabolism -- Chapter 3. Photobiology of Vitamin D -- Chapter 4. The Vitamin D 25-Hydroxylase -- Chapter 5. The 25-Hydroxyvitamin D 1- -Hydroxylase -- Chapter 6. The 25-Hydroxyvitamin D 24-Hydroxylase -- Chapter 7. Mutant Mouse Models of Vitamin D Metabolic Enzymes -- Chapter 8. Vitamin D Binding Protein -- Chapter 9. New Aspects of DBP -- Chapter 10. Endocytic Pathways for 25-(OH) Vitamin D3 -- Section II: MECHANISM OF ACTION -- Chapter 11. The Vitamin D Receptor -- Chapter 12. Vitamin D Receptor Promoter and Regulation of Receptor Expression -- Chapter 13. Nuclear Vitamin D Receptor: Structure-Function, Molecular Control of Gene Transcription, and Novel Bioactions -- Chapter 14. Vitamin D Receptor Cofactors: Function, Regulation, and Selectivity -- Chapter 15. VDR LBD Crystal Structures -- Chapter 16. Comodulators of VDR-Mediated Gene Expression -- Chapter 17. Promoter Targeting of VDR Through A Chromatin Remodeling Complex -- Chapter 18. Molecular Basis of the Diversity of Vitamin D Target Genes -- Chapter 19. Intranuclear Organization of the Regulatory Machinery for Vitamin D-Mediated Control of Skeletal Gene Expression -- Chapter 20. Mouse Models of Vitamin D Receptor Ablation -- Chapter 21. Intranuclear Vitamin D Response Element Binding Proteins -- Chapter 22. VDR and RXR Subcellular Trafficking -- Chapter 23. 1 ,25(OH)2-Vitamin D3 Mediated Rapid and Genomic Responses are Dependent upon Critical Structure-Function Relationships for Both the Ligand and Receptor(s) -- Section III: MINERAL HOMEOSTASIS. , Chapter 24. Vitamin D and the Intestinal Absorption of Calcium: A View and Overview -- Chapter 25. Intestinal Calcium Absorption: Lessons from Knockout Mice and Men -- Chapter 26. Phosphate Homeostasis -- Chapter 27. Mineralization -- Chapter 28. Modeling and Remodeling: How Bone Cells Work Together -- Chapter 29. Vitamin D and the Kidney -- Chapter 30. Vitamin D and the Parathyroids -- Chapter 31. Calcium-Sensing Receptor -- Section IV: TARGET ORGANS AND TISSUES -- Chapter 32. Bone -- Chapter 33. Cartilage and Vitamin D: Genomic and Nongenomic Regulation by 1,25(OH)2D3 and 24,25(OH)2D3 -- Chapter 34. Dento-alveolar Bone Complex and Vitamin D -- Chapter 35. Vitamin D: Role in Skin and Hair -- Chapter 36. Regulation of Immune Responses by Vitamin D Receptor Ligands -- Chapter 37. Vitamin D and Osteoblasts -- Chapter 38. Vitamin D and Osteoclastogenesis -- Chapter 39. Vitamin D Control of the Calcitonin Gene in Thyroid C Cells -- Chapter 40. Vitamin D Regulation of Type I Collagen Expression in Bone -- Chapter 41. Target Genes: Bone Proteins -- Chapter 42. The Calbindins: Calbindin-D9K and Calbindin-D28K -- Chapter 43. Target Genes: PTHrP -- Chapter 44. Effects of 1,25-Dihydroxyvitamin D3 on Voltage-Sensitive Calcium Channels in the Vitamin D Endocrine System -- Chapter 45. Vitamin D and the Cellular Response to Oxidative Stress -- Section V: HUMAN PHYSIOLOGY -- Chapter 46. Vitamin D: Role in the Calcium Economy -- Chapter 47. Effects of Race, Geography, Body Habitus, Diet, and Exercise on Vitamin D Metabolism -- Chapter 48. Perinatal Vitamin D Actions -- Chapter 49. Vitamin D Deficiency and Calcium Absorption During Infancy and Childhood -- Chapter 50. Vitamin D Metabolism and Aging -- Chapter 51. Vitamin D Metabolism in Pregnancy and Lactation -- Chapter 52. Vitamin D and Reproductive Organs. , Chapter 53. Vitamin D Receptor as a Sensor for Toxic Bile Acids -- Chapter 54. Vitamin D and the Renin-Angiotensin System -- Chapter 55. Vitamin D and Muscle -- Chapter 56. Vitamin D and Cardiovascular Medicine -- 9780122526879v2 -- Front Cover -- Vitamin D -- Copyright Page -- Contents -- List of Contributors -- Preface to the 2nd Edition -- Preface to the 1st Edition -- Abbreviations -- Section VI: DIAGNOSIS AND MANAGEMENT -- Chapter 57. Approach to the Patient with Metabolic Bone Disease -- Chapter 58. Detection of Vitamin D and Its Major Metabolites -- Chapter 59. Bone Histomorphometry -- Chapter 60. Radiology of Rickets and Osteomalacia -- Chapter 61. The Pharmacology of Vitamin D, Including Fortification Strategies -- Section VII: DISORDERS OF THE VITAMIN D ENDOCRINE SYSTEM -- Chapter 62. How to Define Normal Values for Serum Concentrations of 25-Hydroxyvitamin D? An Overview -- Chapter 63. Vitamin D and the Pathogenesis of Rickets and Osteomalacia -- Chapter 64. The Hypocalcemic Disorders: Differential Diagnosis and Therapeutic Use of Vitamin D -- Chapter 65. Vitamin D Deficiency and Nutritional Rickets in Children -- Chapter 66. Vitamin D Insufficiency in Adults and the Elderly -- Chapter 67. Vitamin D and Osteoporosis -- Chapter 68. Genetic Vitamin D Receptor Polymorphisms and Risk of Disease -- Chapter 69. Clinical Disorders of Phosphate Homeostasis -- Chapter 70. Disorders of Phosphate Metabolism: Autosomal Dominant Hypophosphatemic Rickets, Tumor Induced Osteomalacia, Fibrous Dysplasia, and the Pathophysiological Relevance of FGF23 -- Chapter 71. Vitamin D Pseudodeficiency -- Chapter 72. Hereditary 1,25-Dihydroxyvitamin D Resistant Rickets -- Chapter 73. Glucocorticoids and Vitamin D -- Chapter 74. Drug and Hormone Effects on Vitamin D Metabolism -- Chapter 75. Bone Disorders Associated with Gastrointestinal &. , Hepatobiliary Disease -- Chapter 76. Vitamin D and Renal Failure -- Chapter 77. Idiopathic Hypercalciuria and Nephrolithiasis -- Chapter 78. Hypercalcemia Due to Vitamin D Toxicity -- Chapter 79. Extra-renal 1 -hydroxylase Activity and Human Disease -- Section VIII: NEW VITAMIN D ANALOGS -- Overview -- Chapter 80. Overview: Rational Design of 1 ,25-Dihydroxyvitamin D3 Analogs (Deltanoids) -- Chapter 81. Analog Metabolism -- Chapter 82. Mechanisms for the Selective Actions of Vitamin D Analogs -- Chapter 83. Molecular Basis for Differential Action of Vitamin D Analogs -- Chapter 84. Development of New Vitamin D Analogs -- Chapter 85. Gemini: The 1,25-dihydroxy Vitamin D Analogs with Two Side-Chains -- Chapter 86. Development of OCT and ED-71 -- Chapter 87. 2-Carbon-Modified Analogs of 19-Nor-1 , 25-Dihydroxyvitamin D3 -- Chapter 88. Non-steroidal Analogs -- Section IX: VITAMIN D AND CANCER -- Chapter 89. Vitamin D: Cancer and Differentiation -- Chapter 90. Vitamin D, Sunlight, and the Natural History of Prostate Cancer -- Chapter 91. Epidemiology of Cancer Risk: Vitamin D and Calcium -- Chapter 92. Differentiation and the Cell Cycle -- Chapter 93. Vitamin D and Breast Cancer -- Chapter 94. Vitamin D and Prostate Cancer -- Chapter 95. Vitamin D and Colon Cancer -- Chapter 96. Vitamin D and Hematological Malignancy -- Chapter 97. Clinical Development of Calcitriol and Calcitriol Analogs in Oncology: Progress and Considerations for Future Development -- Section X: EMERGING USES -- Chapter 98. Vitamin D3: Autoimmunity and Immunosuppression -- Chapter 99. Vitamin D and Diabetes -- Chapter 100. Vitamin D, A Neuroactive Hormone: From Brain Development to Neurodegenerative Disorders -- Chapter 101. Psoriasis and Other Skin Diseases -- Chapter 102. Muscles and Falls -- Chapter 103. Renal Failure and Secondary Hyperparathyroidism. , Chapter 104. Inhibition of Benign Prostatic Hyperplasia by Vitamin D Receptor Ligands -- Index.
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  • 3
    Keywords: Chemistry, Organic. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (516 pages)
    Edition: 1st ed.
    ISBN: 9783709171233
    Series Statement: Fortschritte der Chemie Organischer Naturstoffe Progress in the Chemistry of Organic Natural Products Series ; v.28
    Language: English
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  • 4
    Publication Date: 2018-10-14
    Description: Semiautomated methods for microscopic image acquisition, image analysis, and taxonomic identification have repeatedly received attention in diatom analysis. Less well studied is the question whether and how such methods might prove useful for clarifying the delimitation of species that are difficult to separate for human taxonomists. To try to answer this question, three very similar Fragilariopsis species endemic to the Southern Ocean were targeted in this study: F. obliquecostata, F. ritscheri, and F. sublinearis. A set of 501 extended focus depth specimen images were obtained using a standardized, semiautomated microscopic procedure. Twelve diatomists independently identified these specimen images in order to reconcile taxonomic opinions and agree upon a taxonomic gold standard. Using image analyses, we then extracted morphometric features representing taxonomic characters of the target taxa. The discriminating ability of individual morphometric features was tested visually and statistically, and multivariate classification experiments were performed to test the agreement of the quantitatively defined taxa assignments with expert consensus opinion. Beyond an updated differential diagnosis of the studied taxa, our study also shows that automated imaging and image analysis procedures for diatoms are coming close to reaching a broad applicability for routine use.
    Repository Name: EPIC Alfred Wegener Institut
    Type: Article , isiRev
    Format: application/pdf
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  • 5
    Publication Date: 2019-07-17
    Repository Name: EPIC Alfred Wegener Institut
    Type: Article , isiRev
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  • 6
    Publication Date: 2019-07-17
    Repository Name: EPIC Alfred Wegener Institut
    Type: Article , notRev
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  • 7
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    ELSEVIER SCIENCE BV
    In:  EPIC3Earth and Planetary Science Letters, ELSEVIER SCIENCE BV, 438, pp. 122-129, ISSN: 0012-821X
    Publication Date: 2016-02-15
    Description: Major shifts in ocean circulation are thought to be responsible for abrupt changes in temperature and atmospheric CO2 during the last deglaciation, linked to variability in meridional heat transport and deep ocean carbon storage. There is also widespread evidence for shifts in biological production during these times of deglacial CO2 rise, including enhanced diatom production in regions such as the tropical Atlantic. However, it remains unclear as to whether this diatom production was driven by enhanced wind-driven upwelling or density-driven vertical mixing, or by elevated thermocline concentrations of silicic acid supplied to the surface at a constant rate. Here, we demonstrate that silicic acid supply at depth in the NE Atlantic was enhanced during the abrupt climate events of the deglaciation. We use marine sediment archives to show that an increase in diatom production during abrupt climate shifts could only occur in regions of the NE Atlantic where the deep supply of silicic acid could reach the surface. The associated changes are indicative of enhanced regional wind-driven upwelling and/or weakened stratification due to circulation changes during phases of weakened Atlantic meridional overturning. Globally near-synchronous pulses of diatom production and enhanced thermocline concentrations of silicic acid suggest that widespread deglacial surface-driven breakdown of stratification, linked to changes in atmospheric circulation, had major consequences for biological productivity and carbon cycling.
    Repository Name: EPIC Alfred Wegener Institut
    Type: Article , isiRev
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  • 8
    Publication Date: 2021-05-19
    Description: We present a high-resolution paleoceanographic record of deglaciation based on diatom assemblages from a core located just south of the Polar Front in the southwest Atlantic. Core KC073 is from a sediment drift at the mouth of the Falkland Trough and contains sediments from the Last Glacial Maximum (LGM) to present, dated using radiocarbon dates on bulk organic matter and radiolarian stratigraphy. The site lies along the path of the Antarctic Circumpolar Current (ACC) and immediately downstream of where North Atlantic Deep Water (NADW) is entrained into the ACC. Significant variations in ocean conditions are reflected in high-amplitude changes in diatom concentrations and assemblage composition. The diatom assemblage at the LGM indicates that winter sea ice extent was at least 5° farther north than present until at least 19.0 ka (calendar years) and summer sea ice may have occasionally extended over the site, but for the most part it lay to the south. During deglaciation, Chaetoceros resting spores (CRS) dominate the diatom assemblage with valve concentrations in excess of 500 × 106 valves per gram. Submillennial-scale variations in the numbers of CRS and Thalassiosira antarctica occur throughout the late deglacial and dominate the changes in diatom concentration. We propose that the influx of CRS is controlled by the flow of NADW over the Falkland Plateau. As such our data provide unique evidence that NADW impacted on this sector of the Southern Ocean during deglaciation. During the Holocene the sedimentation rate dramatically reduced. We suggest that the ACC flow increased over the site and inhibited settling and winnowed the surface sediments.
    Description: Published
    Repository Name: AquaDocs
    Type: Journal Contribution , Refereed
    Format: 1-16
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  • 9
    ISSN: 1520-4995
    Source: ACS Legacy Archives
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1520-4995
    Source: ACS Legacy Archives
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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