Arsenic in Soil and Groundwater Environment: Biogeochemical Interactions, Health Effects and Remediation

Bhattacharya, Prosun; Mukherjee, Arun B. B.; Bundschuh, Jochen; Zevenhoven, Ron; Loeppert, Richard H

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Table of contents
  • Cover
  • Table of Contentsvii
  • Prefacexi
  • About the Editorsxv
  • List of Contributorsxxiii
  • Section I: Introduction1
  • Chapter 1. Arsenic in soil and groundwater: an overview3
  • Abstract3
  • 1.1 Introduction4
  • 1.2 Occurrence, distribution, and sources of As5
  • 1.2.1 Occurrence and distribution5
  • 1.2.2 Sources of As in soils and groundwater7
  • 1.2.2.1 Natural sources8
  • 1.2.2.2 Transport and partitioning of As from natural sources8
  • 1.2.3 Anthropogenic sources12
  • 1.2.3.1 Industrial As transport and partitioning13
  • 1.3 Geogenic As in groundwater and soils: a brief overview16
  • 1.3.1 Distribution and chemodynamics of As in groundwater19
  • 1.4 Accumulation and behavior of As in soils28
  • 1.5 Bioaccumulation of As in plants and crops29
  • 1.5.1 Arsenic in crops29
  • 1.5.2 Phytoremediation of As-contaminated soils31
  • 1.6 Speciation and behavior of As in contaminated sites32
  • 1.7 Biogeochemical Controls on As mobilization34
  • 1.8 Health risks associated with chronic exposure to As in groundwater35
  • 1.8.1 Impact of high As ingestion37
  • 1.8.1.1 Social problem38
  • 1.8.2 Treatment39
  • 1.9 Removal of As from drinking water39
  • 1.9.1 Conventional technique40
  • 1.9.2 Other established and emerging arsenic removal method40
  • 1.9.2.1 Pond Sand Filters (PSFs)41
  • 1.9.2.2 Activated alumina filter (ALCAN filter)41
  • 1.9.2.3 Bishuddhya filter42
  • 1.9.2.4 Low cost arsenic removal42
  • 1.9.2.5 Photocatalytic methods42
  • 1.10 Conclusions43
  • References44
  • Section II: Arsenic in Groundwater: Global Occurrences61
  • Chapter 2. Trends in arsenic concentration at tubewells in Bangladesh: conceptual models, numerical63
  • Abstract63
  • 2.1 Introduction63
  • 2.2 The hydrogeological context of As occurrence64
  • 2.2.1 A conceptual model of As in the aquifer66
  • 2.3 Predicting As in tubewell discharge68
  • 2.3.1 Modelling As at shallow HTWs69
  • 2.3.2 Modelling As at DTWs70
  • 2.4 Evidence for changing As concentration at tubewells73
  • 2.4.1 Arsenic concentration and tubewell age in Bangladesh73
  • 2.4.2 Arsenic concentration and tubewell age at village scale74
  • 2.4.3 Time-series monitoring of As concentration76
  • 2.4.4 Isotopic indication of vertical leakage77
  • 2.5 Discussion79
  • 2.6 Future directions80
  • Acknowledgements81
  • References81
  • Chapter 3. Source identification for groundwater arsenic in the Verde Valley, Central Arizona, USA85
  • Abstract85
  • 3.1 Introduction85
  • 3.2 Geology of Verde Valley86
  • 3.2.1 Verde Formation90
  • 3.2.2 Precambrian rocks90
  • 3.2.3 Montezuma Well91
  • 3.2.4 Verde Hot Springs91
  • 3.2.5 Chemical composition of Verde Valley groundwater92
  • 3.2.6 Local channelization of groundwater92
  • 3.3 Experimental92
  • 3.3.1 Cation and anion analyses92
  • 3.3.1.1 ICP–MS analysis93
  • 3.4 Results and discussion93
  • 3.5 Future directions98
  • Acknowledgments98
  • References98
  • Chapter 4. Natural arsenic in groundwater and alkaline lakes at the upper Paraguay basin, Pantanal,101
  • Abstract101
  • 4.1 Introduction102
  • 4.2 Regional setting104
  • 4.3 Materials and methods106
  • 4.3.1 Fieldwork106
  • 4.3.2 Laboratory work108
  • 4.3.2.1 Soil samples108
  • 4.3.2.2 Water samples108
  • 4.3.3 Statistical treatment109
  • 4.3.4 Concentration diagrams109
  • 4.3.5 Thermodynamic modelling109
  • 4.3.6 Residual alkalinity110
  • 4.4 Results111
  • 4.4.1 Soil and water table111
  • 4.4.2 Chemical variability112
  • 4.5 Discussion119
  • 4.5.1 Soil system119
  • 4.5.2 Water table fluctuations120
  • 4.5.3 Chemistry of major elements120
  • 4.5.4 Influences on As122
  • 4.6 Future directions123
  • Acknowledgements124
  • References124
  • Chapter 5. Arsenic in surface- and groundwater in central parts of the Balkan Peninsula (SE Europe)127
  • Abstract127
  • 5.1 Introduction127
  • 5.2 Arsenic in the environment128
  • 5.3 Arsenic in natural waters in the CBP130
  • 5.3.1 Arsenic in surface- and groundwaters130
  • 5.3.2 Arsenic in mineral, thermal, and thermomineral waters138
  • 5.3.2.1 Arsenic in MTWs in Serbia138
  • 5.3.2.2 Arsenic in MTWs in middle-northeast Bosnia144
  • 5.3.2.3 Geochemistry of As-rich MTWs in CBP145
  • 5.4 Environmental impacts146
  • 5.5 Future directions150
  • Acknowledgments151
  • Acronyms and abbreviations151
  • References151
  • Section III: Arsenic in Soil Environment157
  • Chapter 6. Geochemical modelling of arsenic adsorption to oxide surfaces159
  • Abstract159
  • 6.1 Introduction160
  • 6.2 Arsenic adsorption mechanisms161
  • 6.3 Surface complexation modelling of arsenate and arsenite to ferrihydrite and goethite164
  • 6.3.1 Surface complexation models164
  • 6.3.2 Strategy for model optimization167
  • 6.3.3 Modelling arsenate adsorption to ferrihydrite170
  • 6.3.4 Modelling arsenite adsorption to ferrihydrite178
  • 6.3.5 Modelling arsenate adsorption to goethite181
  • 6.3.6 Modelling arsenite adsorption to goethite187
  • 6.4 Arsenate and arsenite adsorption to Al oxides187
  • 6.5 Interactions with other anions and cations189
  • 6.5.1 Interactions with inorganic ions on Fe oxide surfaces – literature evidence189
  • 6.5.2 Interactions with inorganic ions on ferrihydrite – scenarios using generic parameters190
  • 6.5.3 Interactions with organic acids196
  • 6.6 Conclusions200
  • Acknowledgements200
  • References200
  • Chapter 7. Arsenic in the soil environment of central Balkan Peninsula, southeastern Europe: occurre207
  • Abstract207
  • 7.1 Introduction207
  • 7.2 Basic geology and geochemistry of CBP209
  • 7.2.1 Geological framework209
  • 7.2.2 Mineralization and metallogeny209
  • 7.3 Arsenic in CBP lithosphere: rocks, ores, and soils211
  • 7.3.1 Arsenic in rocks and ores211
  • 7.3.2 Arsenic in soils217
  • 7.4 Arsenic in mining and industrial areas219
  • 7.4.1 Arsenic in the environment of mining and metallurgical areas219
  • 7.4.2 Coal-fired power plants225
  • 7.5 Impact of As on biota227
  • 7.5.1 Arsenic in mussels along Danube River227
  • 7.5.2 Soil–plant systems: As in plants227
  • 7.5.3 Emissions of arsenic-rich aerosols from metallurgical facilities and impacts on wild bees229
  • 7.6 Conclusions230
  • 7.7 Future directions231
  • Acknowledgments231
  • References232
  • Chapter 8. Arsenic in soil environments in Albania237
  • Abstract237
  • 8.1 Introduction237
  • 8.2 Materials and methods239
  • 8.2.1 Sampling procedure239
  • 8.2.2 Analytical procedure of soil samples240
  • 8.2.3 Analytical procedure of stream sediment samples240
  • 8.2.4 Quality assurance240
  • 8.3 Arsenic in soils241
  • 8.3.1 The geology of the area241
  • 8.3.2 Arsenic in the soils from sulfide ores area241
  • 8.3.3 Derivation of As from industry244
  • 8.3.4 Soils of Korca area245
  • 8.4 Arsenic in the stream sediments of Albanian rivers247
  • 8.4.1 Study sites247
  • 8.4.2 Arsenic in stream sediment samples248
  • 8.5 Conclusions253
  • References254
  • Chapter 9. Arsenic concentration in selected soils around Abeokuta, southwestern Nigeria257
  • Abstract257
  • 9.1 Introduction257
  • 9.2 The study area258
  • 9.3 Materials and methods260
  • 9.4 Results and discussion260
  • 9.5 Conclusion265
  • Acknowledgments265
  • References265
  • Chapter 10. Levels of trace metals and sequential extraction of arsenic in topsoil and sand from san269
  • Abstract269
  • 10.1 Introduction270
  • 10.2 Multi-elemental sequential extraction270
  • 10.3 Arsenic in soils273
  • 10.3.1 Overview273
  • 10.3.2 Arsenic in impregnated wood274
  • 10.3.3 Arsenic in organisms274
  • 10.4 Methods275
  • 10.4.1 Sampling and sample preparation275
  • 10.4.2 Dissolution – sequential extraction procedure275
  • 10.4.3 Dissolution – total concentration procedure277
  • 10.4.4 Atomic absorption spectrometry277
  • 10.4.4.1 Graphite furnace (As)277
  • 10.4.4.2 Graphite furnace (Cd)278
  • 10.4.4.3 Flame278
  • 10.5 Results and discussion278
  • 10.5.1 Acid-soluble concentrations of seven trace elements in topsoil and sandbox samples at 24 play278
  • 10.5.2 Sequential extraction of arsenic in topsoil and sandbox samples at 24 playgrounds283
  • 10.5.3 Sequential extraction of As in all topsoil samples287
  • 10.6 Summary and conclusions291
  • 10.6.1 Acid-soluble concentrations of seven trace elements in topsoil and sandbox samples at 24 play291
  • 10.6.2 Sequential extraction of As in topsoil and sandbox samples at 24 playgrounds291
  • 10.6.3 Sequential extraction of arsenic in all topsoil samples292
  • Acknowledgements293
  • References293
  • Section IV: Arsenic in Plants and Crops297
  • Chapter 11. Spatial distribution, localization, and speciation of arsenic in the hyperaccumulating F299
  • Abstract299
  • 11.1 Introduction300
  • 11.2 Materials and methods302
  • 11.2.1 Tissue preparation302
  • 11.2.2 X-ray mapping302
  • 11.2.3 X-ray absorption spectroscopy analysis304
  • 11.3 Results304
  • 11.3.1 Macro-distribution of As in different organs304
  • 11.3.2 Micro-distribution of As in the fronds306
  • 11.3.3 Analysis of xylem sap306
  • 11.4 Discussion307
  • Acknowledgments310
  • References310
  • Chapter 12. Arsenic accumulation by Talinum cuneifolium – application for phytoremediation of arse315
  • Abstract315
  • 12.1 Introduction316
  • 12.2 Study area317
  • 12.3 Materials and methods318
  • 12.3.1 Experimental design318
  • 12.3.2 Plant material321
  • 12.3.3 Collection of As-contaminated soil and characterization321
  • 12.3.4 Heavy metal analysis322
  • 12.4 Results and discussion322
  • 12.4.1 Time dependency studies322
  • 12.4.2 Dose–response studies324
  • 12.4.3 Arsenic bioconcentration and translocation factors324
  • 12.4.4 Fractionation studies326
  • 12.4.5 Uptake of As in presence of co-metal ions327
  • 12.4.6 Effect of As uptake in the presence of co-anions and chelators328
  • 12.4.7 Arsenic uptake from contaminated soils of Patancheru330
  • 12.5 Conclusions331
  • 12.6 Future directions332
  • Acknowledgments332
  • References333
  • Chapter 13. Effects of arsenic-contaminated irrigation water, zinc and organic matter on the mobiliz339
  • Abstract339
  • 13.1 Introduction339
  • 13.2 Soil and groundwater quality341
  • 13.2.1 Soil quality341
  • 13.2.2 Groundwater quality344
  • 13.3 Nature and characteristics of the soil under study347
  • 13.4 Experiments on mobilization of As in soils in relation to rice348
  • 13.5 Results and discussions349
  • 13.5.1 Arsenic mobilization in soils350
  • 13.5.1.1 Effect of organic matter350
  • 13.5.1.2 Effect of zinc and other ions351
  • 13.5.1.3 Upper toxic limit of As353
  • 13.5.2 Arsenic accumulation in plants354
  • 13.5.2.1 Effect of methods of As-contaminated water and zinc354
  • 13.5.2.2 Arsenic uptake by crops in sequences and build-up in soil355
  • 13.6 Microbial decontamination of As-contaminated soils through groundwater356
  • 13.7 Future research directions359
  • Acknowledgements360
  • References360
  • Section V: Arsenic in Contaminated Sites (including Mining Wastes)363
  • Chapter 14. Long-Term environmental impact of arsenic-dispersion in Minas Gerais, Brazil365
  • Abstract365
  • 14.1 Introduction366
  • 14.2 Environmental media and pathways: air, soil, and water368
  • 14.2.1 Atmospheric pathway369
  • 14.2.2 Soil pollution370
  • 14.2.3 Water pathway374
  • 14.3 Biota as receptors375
  • 14.3.1 Foodstuff375
  • 14.3.2 Human urine and hair376
  • 14.4 Future directions378
  • Acknowledgements380
  • References380
  • Chapter 15. Processes and conditions affecting elevated arsenic concentrations in groundwaters of Tu383
  • Abstract383
  • 15.1 Introduction384
  • 15.2 Hydrogeologic information384
  • 15.2.1 Hydrogeology of Tulare Lake Hydrologic Region384
  • 15.2.2 Groundwater hydrology and quality389
  • 15.2.3 Climate389
  • 15.3 Groundwater quality and the sources of As390
  • 15.3.1 Shallow groundwater390
  • 15.3.2 Deep groundwater of Hanford392
  • 15.4 Processes and factors affecting As solubility and mobility397
  • 15.4.1 Evapotranspiration398
  • 15.4.2 Geochemical processes398
  • 15.4.2.1 Sorption/desorption399
  • 15.4.2.2 Redox transformation401
  • 15.4.2.3 Speciation and transport403
  • 15.4.3 Agriculture: irrigation and drainage404
  • 15.5 Future directions406
  • References407
  • Chapter 16. Arsenic in soils in the areas of former mining and mineral processing in Lower Silesia,411
  • Abstract411
  • 16.1 Introduction411
  • 16.2 Arsenic-rich ‘‘hot’’ spots in Lower Silesia414
  • 16.2.1 Zloty Stok414
  • 16.2.2 Zelezniak415
  • 16.2.3 Czarnow415
  • 16.3 Materials and methods416
  • 16.3.1 Sampling sites416
  • 16.3.2 Basic soil properties417
  • 16.3.3 Total and soluble As in soils417
  • 16.3.4 Arsenic speciation418
  • 16.4 Results420
  • 16.4.1 Soil properties and As concentrations in soils420
  • 16.4.1.1 Zloty Stok422
  • 16.4.1.2 Zelezniak426
  • 16.4.1.3 Czarnow427
  • 16.4.2 Arsenic solubility427
  • 16.4.3 Plant uptake428
  • 16.4.4 Speciation results429
  • 16.5 Future directions436
  • Acknowledgements437
  • References437
  • Chapter 17. Arsenic speciation and mobility in mine wastes from a copper–arsenic mine in Devon, UK441
  • Abstract441
  • 17.1 Introduction441
  • 17.2 Materials and methods442
  • 17.2.1 Study area442
  • 17.2.2 Methods of As production442
  • 17.2.3 Sample collection and preparation444
  • 17.2.4 Analytical methods444
  • 17.2.4.1 Chemical analysis444
  • 17.2.4.2 Partitioning by sequential extraction444
  • 17.2.4.3 Mineralogical and scanning electron microscopy analysis445
  • 17.2.4.4 X-ray absorption spectroscopy analysis446
  • 17.2.5 Thermodynamic data447
  • 17.3 Results and discussion447
  • 17.3.1 Bulk chemistry of the tailings and mine wastes447
  • 17.3.2 Mineralogic/petrographic characterisation447
  • 17.3.2.1 Sandy tailings447
  • 17.3.2.2 Black furnace slag452
  • 17.3.2.3 Ore crusher area454
  • 17.3.2.4 Efflorescences454
  • 17.3.3 Arsenic partitioning by sequential extractions454
  • 17.3.4 Arsenic speciation by X-ray absorption spectroscopy455
  • 17.3.4.1 X-ray absorption near edge structure spectra455
  • 17.3.4.2 Extended X-ray absorption fine structure spectra462
  • 17.3.5 Arsenic in water leachates465
  • 17.3.6 Thermodynamic calculations465
  • 17.4 Geochemical controls on As mobilisation468
  • 17.5 Future directions468
  • Acknowledgements468
  • References469
  • Chapter 18. Origin and fate of arsenic in a historic mining area of Mexico473
  • Abstract473
  • 18.1 Introduction473
  • 18.2 Mining in Mexico474
  • 18.3 Arsenic in Mexico476
  • 18.4 Arsenic in Zimapán480
  • 18.4.1 Geological framework481
  • 18.4.2 The aquifer system482
  • 18.4.3 Hydrogeochemistry484
  • 18.4.4 Arsenic from mining wastes485
  • 18.4.5 Fate of As486
  • 18.5 Treatment alternatives487
  • 18.5.1 Overview487
  • 18.5.2 Bench-scale jar tests487
  • 18.5.3 Mobile treatment plant490
  • 18.5.4 Geological treatment492
  • 18.6 Future directions493
  • References494
  • Section VI: Biogeochemistry of Arsenic in Soils and Aquatic Environment499
  • Chapter 19. Dynamics of arsenic at hydrothermal spring outlets: role of Fe oxyhydroxides and carbona501
  • Abstract501
  • 19.1 Introduction501
  • 19.2 The study site502
  • 19.2.1 Geography and geological setting502
  • 19.2.2 Spring waters502
  • 19.2.3 The origin of As504
  • 19.3 Observation of the fate of As505
  • 19.4 Dynamics of As: laboratory and field experiments506
  • 19.4.1 Materials and methods506
  • 19.4.1.1 Experimental systems and protocols506
  • 19.4.1.2 Solution characterisation507
  • 19.4.1.3 Precipitate characterisation508
  • 19.4.2 Results and discussion508
  • 19.4.2.1 Cézallier water characterisation508
  • 19.4.2.2 Major element evolution508
  • 19.4.2.3 Dynamics of As510
  • 19.4.2.4 Mechanisms controlling As behaviour510
  • 19.5 Mechanistic approach: geochemical modelling512
  • 19.5.1 Model512
  • 19.5.1.1 Conceptual model512
  • 19.5.1.2 Thermodynamic and kinetic data513
  • 19.5.1.3 Transport modelling515
  • 19.5.2 Modelling results515
  • 19.5.2.1 Simulation of the laboratory experiments (with adjustment of kinetic constants)515
  • 19.5.2.2 Simulation of laboratory experiments (without adjustment of kinetic constants)515
  • 19.5.2.3 Modelling of the ‘‘Fast’’ dynamic field experiments516
  • 19.5.3 Discussion on the modelling results517
  • 19.5.3.1 Laboratory experiment simulation517
  • 19.5.3.2 Field experiment simulation518
  • 19.6 Conclusion and perspectives519
  • References520
  • Section VII: Wastes and Material Flow525
  • Chapter 20. Arsenic flows in the environment of the European Union: a synoptic review527
  • Abstract527
  • 20.1 Introduction528
  • 20.2 Production, uses and emissions of As in the EU-15531
  • 20.2.1 Production of As531
  • 20.2.2 Uses of As531
  • 20.2.3 Atmospheric emission of As533
  • 20.3 Arsenic in soils and landfills540
  • 20.3.1 Behaviour of As in soil compartment540
  • 20.3.2 Arsenic in landfills540
  • 20.4 Summary and conclusions541
  • Acknowledgements542
  • References542
  • Section VIII: Health Risks of Arsenic549
  • Chapter 21. Arsenic in drinking water and bladder cancer: review of epidemiological evidence551
  • Abstract551
  • 21.1 Introduction551
  • 21.2 Arsenic in water553
  • 21.3 Other sources of arsenic554
  • 21.3.1 Arsenic in the diet554
  • 21.3.2 Occupational arsenic exposure558
  • 21.3.3 Arsenic in tobacco559
  • 21.4 Mechanisms of arsenic-induced carcinogenesis559
  • 21.5 Epidemiologic investigations of arsenic and bladder cancer563
  • 21.5.1 Ecologic investigations563
  • 21.5.2 Ecologic cohort investigations566
  • 21.5.3 Individual-level investigations567
  • 21.6 Confounding variables and effect modifiers571
  • 21.6.1 Disinfection byproducts571
  • 21.6.2 Nitrates572
  • 21.6.3 Total fluid intake and urinary stasis572
  • 21.6.4 Micronutrients573
  • 21.6.5 Genetic polymorphisms573
  • 21.7 Future directions574
  • References576
  • Section IX: Arsenic Remediation585
  • Chapter 22. Role of natural red earth in arsenic removal in drinking water – comparison with synth587
  • Abstract587
  • 22.1 Introduction587
  • 22.1.1 Geochemical processes controlling As mobility588
  • 22.1.2 Dominant adsorptive minerals588
  • 22.2 Novel As adsorbent – natural red earth589
  • 22.2.1 Characteristic features of natural red earth589
  • 22.2.1.1 Surface properties of natural red earth591
  • 22.2.1.2 Arsenic adsorption592
  • 22.3 Experimental procedure592
  • 22.3.1 Materials592
  • 22.3.1.1 Sorbent materials592
  • 22.3.1.2 Reagents595
  • 22.3.2 Methods595
  • 22.3.2.1 Adsorption experiments595
  • 22.3.2.2 Model calculations595
  • 22.4 Arsenic adsorption on gibbsite and goethite596
  • 22.4.1 Adsorption edges596
  • 22.4.1.1 Arsenite adsorption596
  • 22.4.1.2 Arsenate adsorption597
  • 22.4.2 Adsorption data modelling597
  • 22.4.3 Use of red earth for the removal of As from drinking water598
  • 22.5 Future directions599
  • Acknowledgements600
  • References600
  • Chapter 23. Household water treatment option: removal of arsenic in presence of natural Fe-containin603
  • Abstract603
  • 23.1 Introduction604
  • 23.2 Materials and methods608
  • 23.2.1 Preparation of stock solutions608
  • 23.2.2 Preparation of synthetic groundwater (test solution)609
  • 23.2.3 Preparation of simulated groundwater (field samples)609
  • 23.2.4 Solar radiation experiments609
  • 23.2.5 Effect of phosphorous612
  • 23.2.6 Experiment with different chelating agents612
  • 23.2.7 Reproducibility613
  • 23.3 Results and discussions613
  • 23.3.1 Groundwater quality of BDP613
  • 23.3.2 Solar radiation experiments615
  • 23.3.3 Chelating agents616
  • 23.3.4 Arsenic removal in presence of phosphate618
  • 23.4 Discussion and conclusion619
  • References620
  • Chapter 24. Arsenite oxidation by ferrate in aqueous solution623
  • Abstract623
  • 24.1 Introduction624
  • 24.2 Experimental section626
  • 24.2.1 Overview626
  • 24.2.2 Materials627
  • 24.2.3 Oxidation of As(III)628
  • 24.2.4 Analysis of As(III) and As(V)628
  • 24.3 Results and discussion628
  • 24.3.1 The effects of oxidizing conditions628
  • 24.3.2 Discussion on possible redox processes632
  • 24.3.3 Correction factor of Fe(VI)634
  • 24.4 Suggestions for further research636
  • Acknowledgments636
  • References637
  • Subject Index643
  • Author Index641
Book details
  • Vendor Elsevier S & T
  • SKU 9780444518200
  • ISBN-13 9780080522906
  • Author Bhattacharya, Prosun; Mukherjee, Arun B. B.; Bundschuh, Jochen; Zevenhoven, Ron; Loeppert, Richard H
  • Category Medical
  • Subject Toxicology

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This volume presents the recent developments in the field of arsenic in soil and groundwater. Arranged into nine sections, the text emphasizes the global occurrences of arsenic in the environment, particularly on its source, pathways, behavior, and effects it has on soils, plants, water, animals, and humans. It also covers the diverse issues of arsenic in the mining environment, arsenic emanating from hydrothermal springs, and the geochemical modeling of arsenic adsorption to oxide surfaces. Finally, the text includes different cost effective removal mechanisms of arsenic from drinking water using natural red earth, solar oxidation, and arsenic oxidation by ferrrate.

Written in simple English, and few technical terms, the book is designed to create interest within the countries with occurrences of arsenic in drinking water with
· an update the current status of knowledge on the dynamics of natural arsenic from the aquifers through groundwater to food chain and efficient techniques for arsenic removal.
· serve as a standard text book for graduate, postgraduate students and researchers in the field of Environmental Sciences and Hydrogeochemistry as well as researchers, environmental scientists and chemists, toxicologists, medical scientists and even for general public seeking an in-depth view of arsenic which had been classed as a carcinogen.
· bring awareness, among administrators, policy makers and company executives, on the problem and to improve the international cooperation