Univariate global Moran’s I result for the years 2000–2015.
\\n\\n
IntechOpen Book Series will also publish a program of research-driven Thematic Edited Volumes that focus on specific areas and allow for a more in-depth overview of a particular subject.
\\n\\nIntechOpen Book Series will be launching regularly to offer our authors and editors exciting opportunities to publish their research Open Access. We will begin by relaunching some of our existing Book Series in this innovative book format, and will expand in 2022 into rapidly growing research fields that are driving and advancing society.
\\n\\nLaunching 2021
\\n\\nArtificial Intelligence, ISSN 2633-1403
\\n\\nVeterinary Medicine and Science, ISSN 2632-0517
\\n\\nBiochemistry, ISSN 2632-0983
\\n\\nBiomedical Engineering, ISSN 2631-5343
\\n\\nInfectious Diseases, ISSN 2631-6188
\\n\\nPhysiology (Coming Soon)
\\n\\nDentistry (Coming Soon)
\\n\\nWe invite you to explore our IntechOpen Book Series, find the right publishing program for you and reach your desired audience in record time.
\\n\\nNote: Edited in October 2021
\\n"}]',published:!0,mainMedia:{caption:"",originalUrl:"/media/original/132"}},components:[{type:"htmlEditorComponent",content:'With the desire to make book publishing more relevant for the digital age and offer innovative Open Access publishing options, we are thrilled to announce the launch of our new publishing format: IntechOpen Book Series.
\n\nDesigned to cover fast-moving research fields in rapidly expanding areas, our Book Series feature a Topic structure allowing us to present the most relevant sub-disciplines. Book Series are headed by Series Editors, and a team of Topic Editors supported by international Editorial Board members. Topics are always open for submissions, with an Annual Volume published each calendar year.
\n\nAfter a robust peer-review process, accepted works are published quickly, thanks to Online First, ensuring research is made available to the scientific community without delay.
\n\nOur innovative Book Series format brings you:
\n\nIntechOpen Book Series will also publish a program of research-driven Thematic Edited Volumes that focus on specific areas and allow for a more in-depth overview of a particular subject.
\n\nIntechOpen Book Series will be launching regularly to offer our authors and editors exciting opportunities to publish their research Open Access. We will begin by relaunching some of our existing Book Series in this innovative book format, and will expand in 2022 into rapidly growing research fields that are driving and advancing society.
\n\nLaunching 2021
\n\nArtificial Intelligence, ISSN 2633-1403
\n\nVeterinary Medicine and Science, ISSN 2632-0517
\n\nBiochemistry, ISSN 2632-0983
\n\nBiomedical Engineering, ISSN 2631-5343
\n\nInfectious Diseases, ISSN 2631-6188
\n\nPhysiology (Coming Soon)
\n\nDentistry (Coming Soon)
\n\nWe invite you to explore our IntechOpen Book Series, find the right publishing program for you and reach your desired audience in record time.
\n\nNote: Edited in October 2021
\n'}],latestNews:[{slug:"step-in-the-right-direction-intechopen-launches-a-portfolio-of-open-science-journals-20220414",title:"Step in the Right Direction: IntechOpen Launches a Portfolio of Open Science Journals"},{slug:"let-s-meet-at-london-book-fair-5-7-april-2022-olympia-london-20220321",title:"Let’s meet at London Book Fair, 5-7 April 2022, Olympia London"},{slug:"50-books-published-as-part-of-intechopen-and-knowledge-unlatched-ku-collaboration-20220316",title:"50 Books published as part of IntechOpen and Knowledge Unlatched (KU) Collaboration"},{slug:"intechopen-joins-the-united-nations-sustainable-development-goals-publishers-compact-20221702",title:"IntechOpen joins the United Nations Sustainable Development Goals Publishers Compact"},{slug:"intechopen-signs-exclusive-representation-agreement-with-lsr-libros-servicios-y-representaciones-s-a-de-c-v-20211123",title:"IntechOpen Signs Exclusive Representation Agreement with LSR Libros Servicios y Representaciones S.A. de C.V"},{slug:"intechopen-expands-partnership-with-research4life-20211110",title:"IntechOpen Expands Partnership with Research4Life"},{slug:"introducing-intechopen-book-series-a-new-publishing-format-for-oa-books-20210915",title:"Introducing IntechOpen Book Series - A New Publishing Format for OA Books"},{slug:"intechopen-identified-as-one-of-the-most-significant-contributor-to-oa-book-growth-in-doab-20210809",title:"IntechOpen Identified as One of the Most Significant Contributors to OA Book Growth in DOAB"}]},book:{item:{type:"book",id:"10631",leadTitle:null,fullTitle:"Vitamin D",title:"Vitamin D",subtitle:null,reviewType:"peer-reviewed",abstract:"This book examines the sometimes controversial role of vitamin D in various health problems. Divided into four sections, chapters cover such topics as vitamin D deficiency in women, newborns, and the elderly, as well as the role of vitamin D in COVID-19, autism spectrum disorder, diabetes, dental diseases, and central nervous system pathological processes.",isbn:"978-1-83969-350-2",printIsbn:"978-1-83969-349-6",pdfIsbn:"978-1-83969-351-9",doi:"10.5772/intechopen.93580",price:119,priceEur:129,priceUsd:155,slug:"vitamin-d",numberOfPages:196,isOpenForSubmission:!1,isInWos:1,isInBkci:!1,hash:"34a58a10957f49842f0b13d78ccacb09",bookSignature:"Öner Özdemir",publishedDate:"September 15th 2021",coverURL:"https://cdn.intechopen.com/books/images_new/10631.jpg",numberOfDownloads:2565,numberOfWosCitations:2,numberOfCrossrefCitations:2,numberOfCrossrefCitationsByBook:0,numberOfDimensionsCitations:3,numberOfDimensionsCitationsByBook:0,hasAltmetrics:1,numberOfTotalCitations:7,isAvailableForWebshopOrdering:!0,dateEndFirstStepPublish:"November 19th 2020",dateEndSecondStepPublish:"December 17th 2020",dateEndThirdStepPublish:"February 15th 2021",dateEndFourthStepPublish:"May 6th 2021",dateEndFifthStepPublish:"July 5th 2021",currentStepOfPublishingProcess:5,indexedIn:"1,2,3,4,5,6",editedByType:"Edited by",kuFlag:!1,featuredMarkup:null,editors:[{id:"62921",title:"Dr.",name:"Öner",middleName:null,surname:"Özdemir",slug:"oner-ozdemir",fullName:"Öner Özdemir",profilePictureURL:"https://mts.intechopen.com/storage/users/62921/images/system/62921.jfif",biography:"Prof. Dr. Oner Ozdemir was born in Alaplı, Zonguldak, Turkey in 1965. He has graduated from İstanbul Medical School, İstanbul University, and become a medical doctor in 1989.\r\nDr. Ozdemir did his pediatric residency at the Department of Pediatrics in Children’s Hospital, İstanbul Medical School, İstanbul, Turkey. His clinical fellowship training was completed at Pediatric Allergy/Immunology division in Louisiana State University, Health Sciences Centre, New Orleans, LA. Some part of his clinical fellowship training was done at the Pediatric Allergy/Immunology program in Cincinnati Children's Hospital Medical Center, Cincinnati, OH. Dr. Ozdemir's bench research areas are as follows: LAK-cell generation and cell-mediated cytotoxicity; human mast cell development and mast cell-mediated cytotoxicity; and apoptosis-related research. Dr. Ozdemir's clinical research areas are as follows: hereditary angioedema, chronic urticaria, biological agents. He was the first place winner of the Clemens Von Pirquet Award from ACAAI at the ACAAI meeting in 2005 for the best research on allergy/asthma/immunology by a fellow in training. Dr. Ozdemir has more than 84 international plus 76 national publications, as well as 174 international and 145 national presentations, and more than 9 chapters related to my research areas. I have been an editor of 4 books so far. Currently, he works as a head of pediatrics and the division of pediatric allergy/immunology at the Medical Faculty of Sakarya University, Sakarya Research and Training Hospital, Adapazarı, Sakarya, Turkey.",institutionString:"Sakarya University",position:null,outsideEditionCount:0,totalCites:0,totalAuthoredChapters:"3",totalChapterViews:"0",totalEditedBooks:"4",institution:{name:"Sakarya University",institutionURL:null,country:{name:"Turkey"}}}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null,coeditorOne:null,coeditorTwo:null,coeditorThree:null,coeditorFour:null,coeditorFive:null,topics:[{id:"379",title:"Vitaminology",slug:"alimentology-vitaminology"}],chapters:[{id:"76108",title:"Vitamin D Metabolism",doi:"10.5772/intechopen.97180",slug:"vitamin-d-metabolism",totalDownloads:418,totalCrossrefCites:0,totalDimensionsCites:1,hasAltmetrics:0,abstract:"Vitamin D plays an important role in bone metabolism. Vitamin D is a group of biologically inactive, fat-soluble prohormones that exist in two major forms: ergocalciferol (vitamin D2) produced by plants in response to ultraviolet irradiation and cholecalciferol (vitamin D3) derived from animal tissues or 7-dehydrocholesterol in human skin by the action of ultraviolet rays present in sunlight. Vitamin D, which is biologically inactive, needs two-step hydroxylation for activation. All of these steps are of crucial for Vitamin D to show its effect properly. In this section, we will present vitamin D synthesis and its action steps in detail.",signatures:"Sezer Acar and Behzat Özkan",downloadPdfUrl:"/chapter/pdf-download/76108",previewPdfUrl:"/chapter/pdf-preview/76108",authors:[{id:"29878",title:"Dr.",name:"Behzat",surname:"Özkan",slug:"behzat-ozkan",fullName:"Behzat Özkan"},{id:"348287",title:"Dr.",name:"Sezer",surname:"Acar",slug:"sezer-acar",fullName:"Sezer Acar"}],corrections:null},{id:"77111",title:"Vitamin D Deficiency in Pregnant Women and Newborn",doi:"10.5772/intechopen.98454",slug:"vitamin-d-deficiency-in-pregnant-women-and-newborn",totalDownloads:159,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:0,abstract:"Vitamin-D is not only an essential element in bone health, but it is also a pro-hormone. Deficiency of vitamin D is the most common cause of rickets and is also known to increase the risk of respiratory distress syndrome, lower respiratory infections, food sensitivities, asthma, type I diabetes, autism and schizophrenia. Vitamin D deficiency limits the effective absorption of dietary calcium and phosphorus. Vitamin D status in newborns is entirely dependent on maternal supply during pregnancy. Low maternal vitamin D status during pregnancy is a major risk factor for rickets in infants. Rickets in children is caused by severe, chronic vitamin D deficiency with apparent skeletal abnormalities, but neonates with vitamin D insufficiency have no overt skeletal or calcium metabolism defects. Rickets was a global disease in the early twentieth century. It has nearly disappeared in developed countries after its causal pathway was understood and fortification of milk with the hormone vitamin D was introduced at the population level. Surprisingly, rickets is re-emerging per recent evidence. Vitamin D deficiency is prevalent in both developed and developing countries. The chapter will review the prevalence of vitamin D deficiency in pregnant women and newborn population and its adverse effects on pregnancy and infant’s health. The chapter also describes evidence-based recommendations to prevent vitamin D deficiency in these vulnerable population.",signatures:"Neelakanta Kanike, Naveen Kannekanti and Jenny Camacho",downloadPdfUrl:"/chapter/pdf-download/77111",previewPdfUrl:"/chapter/pdf-preview/77111",authors:[{id:"342771",title:"M.D.",name:"Neelakanta Kanike",surname:"Kanike",slug:"neelakanta-kanike-kanike",fullName:"Neelakanta Kanike Kanike"},{id:"345979",title:"M.D.",name:"Jenny",surname:"Camacho",slug:"jenny-camacho",fullName:"Jenny Camacho"},{id:"415431",title:"Dr.",name:"Naveen",surname:"Kannekanti",slug:"naveen-kannekanti",fullName:"Naveen Kannekanti"}],corrections:null},{id:"76645",title:"Vitamin D in Elderly",doi:"10.5772/intechopen.97324",slug:"vitamin-d-in-elderly",totalDownloads:197,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:0,abstract:"Vitamin D deficiency is common in elderly people, especially in patients with comorbidity and polypharmcy. In this group, low vitamin D plasma concentration is related to osteoporosis, osteomalacia, sarcopenia and myalgia. Vitamin D status in geriatric population is an effect of joint interaction of all vitamin D metabolic pathways, aging processes and multimorbidity. Therefore, all factors interfering with individual metabolic stages may affect 25-hydroxyvitamin D plasma concentration. The known factors affecting vitamin D metabolism interfere with cytochrome CYP3A4 activity. The phenomenon of drugs and vitamin D interactions is observed first and foremost in patients with comorbidity. This is a typical example of the situation where a lack of “hard evidence” is not synonymous with the possible lack of adverse effects. Geriatric giants, such as sarcopenia (progressive and generalized loss of skeletal muscle mass and strength) or cognitive decline, strongly influence elderly patients. Sarcopenia is one of the musculoskeletal consequences of hypovitaminosis D. These consequences are related to a higher risk of adverse outcomes, such as fracture, physical disability, a poor quality of life and death. This can lead not only to an increased risk of falls and fractures, but is also one of the main causes of frailty syndrome in the aging population. Generally, Vitamin D plasma concentration is significantly lower in participants with osteoporosis and muscle deterioration. In some observational and uncontrolled treatment studies, vitamin D supplementation led to a reduction of proximal myopathy and muscle pain. The most positive results were found in subjects with severe vitamin D deficiency and in patients avoiding high doses of vitamin D. However, the role of vitamin D in muscle pathologies is not clear and research has provided conflicting results. This is most likely due to the heterogeneity of the subjects, vitamin D doses and environmental factors.",signatures:"Malgorzata Kupisz-Urbańska, Jacek Łukaszkiewicz and Ewa Marcinowska-Suchowierska",downloadPdfUrl:"/chapter/pdf-download/76645",previewPdfUrl:"/chapter/pdf-preview/76645",authors:[{id:"341941",title:"Ph.D.",name:"Małgorzata Kupisz-Urbańska",surname:"Kupisz-Urbańska",slug:"malgorzata-kupisz-urbanska-kupisz-urbanska",fullName:"Małgorzata Kupisz-Urbańska Kupisz-Urbańska"},{id:"344068",title:"Prof.",name:"Ewa",surname:"Marcinowska-Suchowierska",slug:"ewa-marcinowska-suchowierska",fullName:"Ewa Marcinowska-Suchowierska"},{id:"348718",title:"Prof.",name:"Jacek",surname:"Łukaszkiewicz",slug:"jacek-lukaszkiewicz",fullName:"Jacek Łukaszkiewicz"}],corrections:null},{id:"76203",title:"Vitamin D and the Immune System",doi:"10.5772/intechopen.97300",slug:"vitamin-d-and-the-immune-system",totalDownloads:160,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:1,abstract:"In the past few decades, various novel actions of vitamin D have been discovered. The mechanism of action of calcitriol or vitamin D is mediated by the Vitamin D receptor (VDR), a subfamily of nuclear receptors, which acts as a transcription factor in the target cells after formation of a heterodimer with the retinoid X receptor (RXR). As the VDR has been found in virtually all cell types, vitamin D exerts multiple actions on different tissues. Vitamin D has important immunomodulatory actions, which includes enhancement of the innate immune system and inhibition of the adaptative immune responses. These actions are associated with an increase in production of interleukin (IL)-4 by T helper (Th)-2 lymphocytes and the up-regulation of regulatory T lymphocytes. Vitamin D can regulate the immune responses in secondary lymphoid organs as well as in target organs through a number of mechanisms. Vitamin D inhibits the expression of APC cytokines, such as interleukin-1 (IL-1), IL-6, IL-12, and tissue necrosis factor- α (TNF-α) and decreases the expression of a set of major histocompatibility complex (MCH) class II cell surface proteins in macrophages. Vitamin D also inhibits B cell differentiation and antibody production. These actions reflect an important role of Vitamin D in balancing the immune system.",signatures:"Vikram Singh Chauhan",downloadPdfUrl:"/chapter/pdf-download/76203",previewPdfUrl:"/chapter/pdf-preview/76203",authors:[{id:"343781",title:"Dr.",name:"Vikram Singh",surname:"Chauhan",slug:"vikram-singh-chauhan",fullName:"Vikram Singh Chauhan"}],corrections:null},{id:"75266",title:"Viral Infections, Including Influenza and Corona Virus Disease 2019, and Vitamin D: A Mini-Review",doi:"10.5772/intechopen.96102",slug:"viral-infections-including-influenza-and-corona-virus-disease-2019-and-vitamin-d-a-mini-review",totalDownloads:221,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:0,abstract:"Recent research about the influence of vitamin D (VD) deficiency on the occurrence of viral infections suggests that children with VD deficiency have attenuated immune response. This, in turn, increases the severity of viral infections, especially those of the respiratory tract, that show a typical seasonality pattern during the winter months. Despite the immunization of children at the global level, outbreaks of influenza do frequently occur. Over the past months, we have witnessed that the explosive pandemic of the corona virus disease 2019 (COVID-19) has caused significant mortality in some countries. Numerous studies have shown that VD deficiency is increasingly prevalent worldwide, and that it is potentially associated with the onset of viral infections. Persons with hypovitaminosis D and subsequent secondary immunodeficiencies ought to be identified and treated, while preventive supplementation of VD should be recommended to the general population to avoid VD deficiency during the winter. In this way, the burden of viral infections on population health and economy could be reduced. This paper also reviews the influence of VD on infections caused by hepatitis B and C viruses, human papillomavirus, Epstein–Barr virus, Human herpes virus 6, herpes simplex virus, and human immunodeficiency virus.",signatures:"Srđana Čulić",downloadPdfUrl:"/chapter/pdf-download/75266",previewPdfUrl:"/chapter/pdf-preview/75266",authors:[{id:"341703",title:"Prof.",name:"Srđana",surname:"Čulić",slug:"srdjana-culic",fullName:"Srđana Čulić"}],corrections:null},{id:"76246",title:"Vitamin D and Its Relationship with the Pathways Related to Thrombosis and Various Diseases",doi:"10.5772/intechopen.97299",slug:"vitamin-d-and-its-relationship-with-the-pathways-related-to-thrombosis-and-various-diseases",totalDownloads:483,totalCrossrefCites:1,totalDimensionsCites:1,hasAltmetrics:1,abstract:"Vitamin D known for its vital role in diverse biological function such as calcium and phosphorus homeostasis, also exert an anticoagulant effect emphasizing its essential role in the thrombosis pathogenesis. Thrombosis is the formation and propagation of a blood clot or thrombus either in the arterial or the venous system resulting in several severe complications. Various studies have also reported the association of vitamin D deficiency with the increased incidences of thromboembolism. This may be in part due to its anticoagulant effects through upregulation of thrombomodulin, an anticoagulant glycoprotein, and downregulation of Tissue Factor, a critical coagulation factor. The protective effects of vitamin D and its receptor in endothelial cells may further explain some of the reported beneficial effects of vitamin D in the prevention or treatment of cardiovascular diseases. Additionally, the immunomodulatory role of vitamin D has been observed through its ability to alter the secretion of inflammatory cytokines that can induce a procoagulant milieu by multiple pathways. Therefore, it becomes pertinent to discuss the close link between vitamin D and human health and to improve our knowledge of the molecular pathways regulated or influenced by vitamin D and its associated metabolites.",signatures:"Syed Mohd, Swati Sharma, Aastha Mishra and Mohammad Zahid Ashraf",downloadPdfUrl:"/chapter/pdf-download/76246",previewPdfUrl:"/chapter/pdf-preview/76246",authors:[{id:"237259",title:"Prof.",name:"Mohammad Zahid",surname:"Ashraf",slug:"mohammad-zahid-ashraf",fullName:"Mohammad Zahid Ashraf"},{id:"344392",title:"Mr.",name:"Syed",surname:"Mohd",slug:"syed-mohd",fullName:"Syed Mohd"},{id:"344393",title:"Dr.",name:"Aastha",surname:"Mishra",slug:"aastha-mishra",fullName:"Aastha Mishra"},{id:"348567",title:"Dr.",name:"Swati",surname:"Sharma",slug:"swati-sharma",fullName:"Swati Sharma"}],corrections:null},{id:"77094",title:"Vitamin D and Dentistry",doi:"10.5772/intechopen.98471",slug:"vitamin-d-and-dentistry",totalDownloads:182,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:0,abstract:"Vitamin D deficiency is a pandemic issue due to decreased vitamin D intake from food and lessened sunlight exposure. Attention is drawn to vitamin D and its role learned in notable clinical disorders such as diabetes, cardiovascular disease and cancers including oral ones. Vitamin D is also very effective along with minerals in the protection of oral health. Vitamin D helps maintain the calcium-phosphate balance and contributes to the shaping of the bone. It is reported that with sufficient vitamin D level, the onset and progression of caries in the tooth structure can be stopped, the formation of caries can be reduced and enamel loss can be prevented. Vitamin D also affects the disease and health conditions of the periodontium. Anti-inflammatory and immunomodulatory functions have a role in the pathogenesis of periodontal disorders. It can reduce bone resorption and suppress the inflammatory outcome related to periodontal diseases by increasing mineral density. Vitamin D has been linked with tooth decay, gingivitis, and tooth loss. Vitamin D, in particular, as a promising oral health-protective agent, is said to lessen the incidence of caries and periodontitis.",signatures:"Elif Gül Aydın and Öner Özdemir",downloadPdfUrl:"/chapter/pdf-download/77094",previewPdfUrl:"/chapter/pdf-preview/77094",authors:[{id:"62921",title:"Dr.",name:"Öner",surname:"Özdemir",slug:"oner-ozdemir",fullName:"Öner Özdemir"},{id:"350883",title:"Dr.",name:"Elif",surname:"Gül Aydin",slug:"elif-gul-aydin",fullName:"Elif Gül Aydin"}],corrections:null},{id:"75800",title:"The Importance of Vitamin D for Periodontal Tissues",doi:"10.5772/intechopen.96968",slug:"the-importance-of-vitamin-d-for-periodontal-tissues",totalDownloads:207,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:0,abstract:"There are many causes of vitamin D deficiency, which determines pathogenesis of many diseases, including periodontal ones. Constant low uptake or deficiency of vitamin D results in progression of periodontal diseases and jaw bone metabolism - leads to change of bone mineral density, causes resorption in alveolar bone, tooth loss, changes of masticatory function and osteoporosis. The clinical studies strive to link vitamin D with gingivitis and periodontitis and prove its therapeutic and preventive role, because of vitamin D immunomodulatory, anti-inflammatory and antiproliferative effects for periodontal tissues and best treatment outcome. The purpose of this chapter is to analyze the importance of vitamin D on the pathogenesis of periodontal diseases, its role on regulation of the immune system and defense mechanism, influence on jawbone quality and on the correlation between vitamin D concentration in plasma and periodontal diseases.",signatures:"Egle Jagelaviciene",downloadPdfUrl:"/chapter/pdf-download/75800",previewPdfUrl:"/chapter/pdf-preview/75800",authors:[{id:"308381",title:"Dr.",name:"Egle",surname:"Jagelaviciene",slug:"egle-jagelaviciene",fullName:"Egle Jagelaviciene"}],corrections:null},{id:"76020",title:"Vitamin D and Diabetic Foot",doi:"10.5772/intechopen.97115",slug:"vitamin-d-and-diabetic-foot",totalDownloads:175,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:0,abstract:"Approximately 15% of patients with diabetes mellitus (DM) are prone to developing diabetic foot ulcers (DFU) in their lifetime. The term vitamin D status or 25-hydroxyvitamin D [25(OH)D] levels are used interchangeably to represent the status of vitamin D in individuals throughout this paper. Evidence suggests a relationship between 25(OH)D levels and DFU. However, very minimal data is available on the association between DFU and vitamin D deficiency. After a careful review of the literature, it was inferred that vitamin D could be associated with DFU and diabetic foot infections. Available evidence on vitamin D and DFU suggests a negative correlation between 25(OH)D levels and the presence of DFU. Evidence also supports a negative relationship between 25(OH)D levels and diabetic foot infections. Further large-scale randomized controlled studies need to be done to confirm the relationship between 25(OH)D levels and DFU including the use of vitamin D in the management of DFU and diabetic foot infections.",signatures:"Antony Macido",downloadPdfUrl:"/chapter/pdf-download/76020",previewPdfUrl:"/chapter/pdf-preview/76020",authors:[{id:"343282",title:"Dr.",name:"Antony",surname:"Macido",slug:"antony-macido",fullName:"Antony Macido"}],corrections:null},{id:"77126",title:"The Role of Vitamin D in Neurodegeneration and Other Pathological Processes of the Central Nervous System",doi:"10.5772/intechopen.98390",slug:"the-role-of-vitamin-d-in-neurodegeneration-and-other-pathological-processes-of-the-central-nervous-s",totalDownloads:159,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:0,abstract:"The nervous system is the most complex organ in the human body, and it is the most essential. However nerve cells are particularly precious as, only like muscle cells, once formed, they do not replicate. This means that neural injuries cannot easily be replaced or repaired. Vitamin D seems to play a pivotal role in protecting these vulnerable and most important structures, but exactly how and to what extend is still subject to debate. Systematically reviewing the vast body of research on the influence of Vitamin D in various neuropathological processes, we found that Vitamin D particularly plays a mitigating role in the development of chronic neurodegeneration and the measured response to acutely acquired traumatic and non-traumatic nerve cells incidents. Adequate serum levels of Vitamin D before the initiation of these processes is increasingly viewed as being neuroprotective. However, comprehensive data on using it as a treatment during the ongoing process or after the injury to neurons is completed are much more ambiguous. A recommendation for testing and supplementation of insufficiencies seems to be well-founded.",signatures:"Carl Nikolaus Homann",downloadPdfUrl:"/chapter/pdf-download/77126",previewPdfUrl:"/chapter/pdf-preview/77126",authors:[{id:"344847",title:"Prof.",name:"Carl Nikolaus",surname:"Homann",slug:"carl-nikolaus-homann",fullName:"Carl Nikolaus Homann"}],corrections:null},{id:"75898",title:"Vitamin D and Autism Spectrum Disorder",doi:"10.5772/intechopen.96928",slug:"vitamin-d-and-autism-spectrum-disorder",totalDownloads:206,totalCrossrefCites:1,totalDimensionsCites:1,hasAltmetrics:0,abstract:"1,25(OH)2D is the hormonally active form of vitamin D known for its pleiotropic immunomodulatory effects. Via altering gene transcription, 1,25(OH)D exerts immunosuppressive effects and stimulates immune regulation. Recently, the interest in vitamin D in association with autism spectrum disorder (ASD) has been triggered. The prevalence of ASD has increased excessively over the last few decades, emphasizing the need for a better understanding of the etiology of the disorder as well as to find better treatments. Vitamin D levels in ASD patients are observed to be lower compared to healthy individuals and maternal vitamin D deficiency has been associated with an increased risk of ASD. Moreover, vitamin D supplementation improves ASD symptoms. These recent clinical findings strongly suggest that vitamin D is a factor in ASD onset and progression. Yet, possible mechanisms behind this association remain unknown. This review summarizes immunomodulatory properties of vitamin D and peripheral immune dysregulation in ASD, after which possible mechanisms via which vitamin D could rebalance the immune system in ASD are discussed. Although promising clinical results have been found, further research is necessary to draw conclusions about the effect and mechanisms behind the effect of vitamin D on ASD development.",signatures:"Maud Vegelin, Gosia Teodorowicz and Huub F.J. 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Venkateswarlu",coverURL:"https://cdn.intechopen.com/books/images_new/371.jpg",editedByType:"Edited by",editors:[{id:"58592",title:"Dr.",name:"Arun",surname:"Shanker",slug:"arun-shanker",fullName:"Arun Shanker"}],productType:{id:"1",chapterContentType:"chapter",authoredCaption:"Edited by"}}]},chapter:{item:{type:"chapter",id:"77399",title:"Geospatial Clustering of Mobile Phone Use and Tuberculosis Health Outcomes among African Health Systems",doi:"10.5772/intechopen.98528",slug:"geospatial-clustering-of-mobile-phone-use-and-tuberculosis-health-outcomes-among-african-health-syst",body:'Mobile phones are becoming increasingly available and accessible globally. The global mobile phone subscription in 2009 was 68.0 per 100 inhabitants compared to 108 in 2019 corresponding to an overall 96% penetration rates1. In the African region, the estimated mobile phone penetration rate was 32.2% in 2008 compared to 85% in 2019 and is projected to rise to over 90% by 2025. The mobile broadband penetration rate also increased from 1.7% in 2008 to 30% in 2019 [1]. Many people who could not access fixed telephones for health informatics now use the mobile phone technology to access health services (mHealth). Compared to the wired information technology, the wireless technology is less expensive, more convenient, and readily accessible for individuals in many developing countries, including African countries [2, 3]. The mobile wireless technology has opportunities to facilitate communication among geographically isolated communities and could be harnessed to improve population health.
Mobile phones brought new opportunities for public health to Sub-Saharan Africa. With most of the African population in rural areas, mobile phone use has facilitated infectious disease management irrespective of geographical barriers [4, 5, 6]. Tuberculosis (TB) management is one area in which mobile phone use has shown great success because to effectively treat TB, patients must take four pills of anti-tuberculosis medications five times per week, for a period of 6 months [7]. This may create a high level of non-compliance to prescribed medications. Such protracted adherence could be facilitated by removing barriers to access and utilization through mHealth technologies [8]. In 2002, the South African government introduced the use of the mHealth technology, and computer databases to optimize TB treatment adherence. The database repeatedly lists patients who are due for their medications and an automatic Short-Message-Service (SMS) reminder sent to their mobile phones. This model enhanced treatment adherence and completion rates among sampled patients [7]. Thus, mobile phones provide platforms through which the SMS technology and other treatment-reminder protocols can be harnessed by TB patients to improve efficiency and optimize outcomes [6, 8]. Our study assumed that increased mobile phone use translates to broader access to TB services and represents the potential for impact on health with utilization of mobile phones to send/receive TB-related health information [9].
This study provides insight into the geospatial clustering of TB and mobile phone use among African health systems. Using an Exploratory Spatial Data Analytic (ESDA) approach, this study explored the spatial relationships between TB treatment completion rates and mobile phone use. Geospatial analytics of these concepts have opportunities to inform TB surveillance, intervention mapping and resource allocation. Moonan et al. conducted a geospatial epidemiological TB surveillance among newly diagnosed TB patients at the Tarrant County Health Department, Fort Worth, Dallas. Their model facilitated the identification of TB transmissions not identified during routine contact tracing. Thereby enabling the identification of at-risk populations, with an intervention mapping recommended for screening, treatment, and rehabilitation [10].
Conceptually, mobile phones facilitate information exchange and transfer without spatial barriers at high efficiency and low cost [4, 5]. Chadha et al. evaluated the effectiveness of the ComCare mobile application in coordinating TB referrals among patients in the Khunti District of India. It was discovered that the mobile technology increased provider accountability and led to improved patient referral, retention, and treatment completion rates among network members [11]. Other researchers showed similar successes demonstrating the use of geospatial analytics in TB control, prevention, and management. Mwila and Phiri using geospatial analyses, cloud computing and web technologies modeled TB prevention strategies among developing countries. They explored ways to optimize TB monitoring and tracking protocols using technologies that display geographic distribution of TB cases on an mHealth application, while providing policy reports to inform intervention mapping activities [12]. While Yakam et al. spatially identified smear-positive pulmonary TB clusters among poor neighborhoods in Douala, Cameroon using mHealth technologies; Herrero et al. spatially explored cluster patterns of TB nonadherence and treatment dropouts in the metropolitan area of Buenos Aires, Argentina. Risk areas of nonadherence were characterized by poverty, ignorance, and reduced access to mHealth technologies [13, 14].
Multiple studies have documented the impact of mobile phone use on TB health outcomes for varied settings [11, 12, 13, 14]. However, it is not immediately clear of the geospatial clustering patterns of TB treatment completion rates and mobile phone use among African countries. Previous studies have focused on evaluating TB medication access using geospatial disaggregated datasets of population characteristics [13, 15]. Hassarangsee et al. investigated the spatial detection and management of TB using information systems in the Si Sa Ket Province, Thailand [16]. However, the focus of this study is to evaluate the geospatial clustering patterns of TB treatment completion rates and mobile phone use among African health systems. It presents an exploratory spatial analysis of the relationships between TB treatment completion rates and mobile phone use for the countries in Africa. Using an ESDA approach to identify countries with low TB treatment completion rates and reduced mobile phone use could be the first step towards addressing issues related to poor TB outcomes. Thus, this presents an opportunity to identify African countries with limited resources and a high need for a wireless technology intervention.
Data for TB outcome and mobile phone use for African countries were obtained from the World Bank database [17] for the periods 2000 through 2015 (Supplementary Material—A). This study excluded one country due to incomplete data. In total, 53 countries representative of the African continent were included in this study. De-identified information was collated and aggregated per country and published at the end of each year by the World Bank, qualifying it as Institutional Review Board exempt [18].
ArcGIS and GeoDa statistical software were used in all geospatial analyses which were performed in three stages and completed in November 2020. Univariate local Moran’s I and global Moran’s I were run on TB treatment completion rates separately. This was followed by a differential local Moran’s I analysis to ascertain differential cluster patterns for different time-periods. Finally, spatial relationships between TB treatment completion rates and mobile phone use for year 2015 was evaluated using ESDA. To investigate treatment completion cluster patterns, spatial and tabular data were uploaded into ArcGIS 10.5.1. Geographically referenced data for TB treatment completion rates and mobile phone use for four time-periods (2000, 2005, 2010, 2015) were extracted for each country. These were added and joined to the African map by country shapefile and analyzed using an ESDA approach to visualize patterns and trends among geographically referenced data.
The Local Indicator of Spatial Association (LISA) represents the localized equivalent of the global Moran’s I [19, 20]. For any location on a map, the LISA statistic measures and statistically tests the similarity of the geographically referenced data for that location (e.g., TB treatment completion rates at the source country) with the values of its corresponding local neighbors in space (surrounding countries). According to standard practice for reporting geospatial analytics, positive spatial autocorrelation is placed into High-High and Low-Low clusters; and negative spatial autocorrelation is placed into High-Low and Low-High outliers. High-High clusters denote above-average values of core countries versus surrounding countries. Low-Low clusters represent below average values of core countries versus surrounding countries. Low-High clusters means small changes among core countries versus high changes in the surrounding countries. Conversely, High-Low clusters means high changes among core countries versus small changes in the surrounding countries [20, 21]. For this study, a randomization of 999 permutations was used prior to result interpretations, and this study only analyzed observations with neighbors [20, 21, 22].
The Local Differential Moran’s I (LDMI) statistic Eq. (1) measures if a variable change in space over time is related to its neighbors, and is calculated thus:
Where
Using geospatial data for 53 African countries for the periods 2000–2015, univariate global Moran’s I values and associated pseudo p-values were computed and documented (Supplementary Material—B). In addition, LISA analytics identified different cluster patterns (Low-Low and High-Low) that were significant at different p-values (Table 1).
Figure 1 shows the clusters and significance levels of TB treatment completion rates in year 2000. Thirteen countries had significant clusters at different p-values including:
Clusters and significance levels of TB treatment completion rates in year 2000.
Figure 2 represents the clusters and significance levels of TB treatment completion rates in year 2005. Nine countries had significant cluster patterns at different p-values.
Clusters and significance levels of TB treatment completion rates in year 2005.
The clusters and significance levels of TB treatment completion rates for year 2010 are shown in Figure 3. Eight countries had significant clusters at different p-values.
Clusters and significance levels of TB treatment completion rates in year 2010.
The cluster patterns and significance levels of TB treatment completion rates for year 2015 are shown in Figure 4. Eight countries had significant clusters at different p-values.
Clusters and significance levels of TB treatment completion rates in year 2015.
LDMI analytics identified different cluster patterns for the different time periods evaluated (Tables 2–4).
Variables | Moran’s I value | Pseudo p-value | |
---|---|---|---|
TB_TreatmentCompletionRate_Yr2000 | 0.0190 | 0.021 | |
Univariate Global Moran’s I | TB_TreatmentCompletionRate_Yr2005 | 0.0177 | 0.032 |
TB_TreatmentCompletionRate_Yr2010 | 0.0196 | 0.025 | |
TB_TreatmentCompletionRate_Yr2015 | 0.0179 | 0.031 |
Univariate global Moran’s I result for the years 2000–2015.
Countries | Cluster Type | |
---|---|---|
Variable: TB_2000 & 2005 | Algeria | High-Low* |
Burkina Faso | Low-Low* | |
Senegal | Low-Low** |
Differential local Moran’s I estimations of TB treatment completion rates between time 0 (2000) and time 1 (2005).
Significance level: *p < 0.05; **p < 0.01.
Variable: TB_2000 & 2010 | Countries | Cluster Type |
---|---|---|
Niger | Low-Low* | |
Senegal | Low-Low** | |
Gambia | Low-Low** | |
Namibia | Low-High* | |
Lesotho | Low-High* | |
Djibouti | Low-High* | |
Algeria | High-Low* | |
Cameroon | High-Low* | |
South Africa | High-Low* | |
Dem Rep Congo | High-High* | |
Kenya | High-High* | |
Sierra Leone | High-High* |
Differential local Moran’s I estimations of TB treatment completion rates between time 0 (2000) and time 2 (2010).
Significance level: *p < 0.05; **p < 0.01.
Variable: TB_2000 & 2015 | Countries | Cluster Type |
---|---|---|
Niger | Low-Low* | |
Burkina Faso | Low-Low* | |
Senegal | Low-Low*** | |
South Africa | Low-Low** | |
Algeria | High-Low** | |
Cameroon | High-Low** | |
Dem Rep Congo | High-High** |
Differential local Moran’s I estimations of TB treatment completion rates between time 0 (2000) and time 3 (2015).
Significance level: *p < 0.1; **p < 0.05; ***p < 0.01.
Table 2 represents LDMI results between time 0 (2000) and time 1 (2005). Algeria, Burkina Faso, and Senegal had significant clusters at different p-values (Supplementary Material—C).
Table 3 shows the result between time 0 (2000) and time 2 (2010). Niger, Senegal, Gambia, Namibia, Lesotho, Djibouti, Algeria, Cameroon, South Africa, Democratic Republic of Congo (DRC), Kenya, and Sierra Leone had significant clusters at different p-values (Supplementary Material—C).
Table 4 represents estimation results between time 0 (2000) and time 3 (2015). Niger, Burkina Faso, Senegal, South Africa, Algeria, Cameroon, and DRC had significant clusters at different p-values (Supplementary Material—C).
Spatial relationship between TB treatment completion rates and mobile phone use identified High-High clusters, Low-Low clusters, and Low-High outliers (Figure 5).
Spatial correlation result between TB treatment completion rates and Mobile phone use.
Differential local Moran’s I estimations of TB treatment completion rates between time 0 (2000) and time 1 (2005).
ESDA identified statistically significant clusters in TB treatment completion rates among some countries of Africa. Most African countries except those in the Southern region had significant clusters (Figures 1–4), predominantly Low-Low clusters (14 countries) and High-Low clusters (10 countries). Low-Low clusters suggest that TB treatment completion rates between 2000 and 2015 were low among identified countries and were surrounded by countries with similar low changes. High-Low clusters suggest high changes in the core countries versus low changes in their surrounding countries (18, 19). In year 2000, Algeria had a “High-Low” cluster tract (Figure 1). This suggests that the TB treatment completion rates for Algeria in 2000 was high, surrounded by countries with low rates. DRC had a “Low-Low” cluster tract in year 2010; suggesting that TB treatment completion rates was low for DRC, surrounded by countries with similar low changes (Figure 3). These findings could inform the formation of health policies for TB management strategies including resource allocation frameworks in countries. Study results also indicated that only a few countries had complete treatments for TB across Africa within the period of this study analyses. 13 countries out of 53 (Figure 1) had treatment completion rates in the year 2000, with all clusters being either outliers or cold spots. Nine countries in 2005 (Figure 2), eight countries in 2010 (Figure 3), and eight countries in 2015 (Figure 4). These suggest that poor compliance and nonadherence could impact treatment completion rates for which the mHealth technology could be harnessed to address issues related to access, utilization, and attrition [8, 14].
Differential local Moran’s I estimations of TB treatment completion rates between time 0 (2000) and time 2 (2010).
Differential local Moran’s I estimations of TB treatment completion rates between time 0 (2000) and time 3 (2015).
Differential Moran’s I cluster maps identified hot spots, cold spots, and outliers among African countries. The base-case analysis identified three countries with significant clusters including Algeria, Burkina Faso, and Senegal. Cluster patterns for Burkina Faso and Senegal were Low-Low cluster tracts, which suggest low TB treatment completion rates surrounded by countries with similar low changes. Conversely, Algeria had High-Low clusters suggesting high changes in TB treatment completion rates versus low changes in surrounding countries (Supplementary Material—C, Figure 6). These findings could inform planning and suggest that the mHealth technology have opportunities to improve outcomes by facilitating fast, reliable, and updated health information.
While the time-period 2 analysis identified 12 countries with High-High clusters (Supplementary Material—C, Figure 7); the time-period 3 analysis identified eight countries with significant clusters (Supplementary Material—C, Figure 8). Altogether, two countries including Algeria and Senegal had significant clusters across the three time-periods of study evaluation (Supplementary Material—C). Nonetheless, of note is the fact that only three countries had significant clusters from LDMI analytics in year 2005 (Supplementary Material—C, Figure 6), compared to 2010 and 2015 where 12 countries (Supplementary Material—C, Figure 7) and seven countries (Supplementary Material—C, Figure 8) had significant clusters respectively. A possible explanation could be that 5-year period may not be enough time to appreciate significant changes in TB treatment rates (23). Conversely, the 15-year period may be too long to observe this trend. Thus, it appears the ideal time for this evaluation should be around 10-year time-periods. This gives credence to treatment guideline policy change introduced in 2009 by WHO that advocates following patients post treatment for longer periods irrespective of the form of TB [23]. In view of this, future studies should aim to do a sensitivity analysis to determine the precise time to explore TB treatment completion rates among African health systems.
It must be noted that identifying significant clusters in TB treatment completion rates in any country does not translate to TB-free nations. South Africa is one of the nations with good TB programs in Africa [22], corroborating this study findings (Tables 2–4). South Africa had significant clusters for TB treatment completion rates (Supplementary Material—C); which could possibly be attributed to the coordinated TB control measures introduced by the South African government [7]. However, despite government efforts to curb the incidence of TB in South Africa, recent study by the WHO identified South Africa as one of the seven countries that accounted for 64% of global new cases of TB [24]. Thus, notwithstanding significant TB treatment completion clusters identified by this study, the burden of TB in South Africa remains high.
Exploratory spatial data analyses identified significant association between TB treatment completion rates and mobile phone use rates. Countries with higher rates of mobile phone use, showed higher TB treatment completion rates suggesting enhanced program uptake. Dissecting this association with local level geographical data revealed differing cluster patterns suggesting that the diffusion was not consistent across the region.
High-High clusters indicate countries with high TB treatment completion rates surrounded by countries with similar high mobile phone use rates. Tunisia, Sierra Leone, Eritrea, Kenya, Rwanda, Tanzania, and Mozambique had High-High clustering of these two attributes (Figure 5). This suggests that the use of mobile phones may be facilitating TB treatment completion rates; and gives credence to findings by Chadha et al. which demonstrated how the mobile phone technology strengthened and optimized TB health outcomes [11].
Low-Low clusters indicate countries with low TB completion rates surrounded by countries with low mobile phone use rates. Mauritania, Nigeria, Cameroon, Equatorial Guinea, Gabon, Angola, and South Africa had significant Low-Low clustering of these two attributes (Figure 5). Such low uptakes may be contributory to the high burden of TB in Nigeria and South Africa and lends credence to reports by WHO that listed them among the six countries that contributed to the high burden of global new cases of TB in 2017 [24].
Spatial outliers indicate countries with either high or low TB completion rates surrounded by countries with either low or high mobile phone use rates. Identified Low-High outliers include Zimbabwe, Somalia, Ethiopia, Libya, Sudan, and Uganda (Figure 5). These are potential moderators and mediators for this study; and could possibly be related to factors that impede the use of mobile phones for health informatics including poverty, ignorance, and poor access to mHealth technologies [14].
This study had some limitations. It did not control for the presence or absence of factors that could influence access and utilization of services, which could impact the robustness of study findings. In addition, there were some limitations in the datasets used for this study. Geographical data for TB cases from the World Bank were at the country level only– granular spatial relationships could have been used and would have revealed cases at a finer resolution. More so, this study is exploratory in nature. It assesses correlation and not causation and becomes the first step in assessing the relationship between TB health outcomes and potential impacts of ICT tools such as mobile phone use on TB programs among African health systems.
Evidence-based decision making, monitoring of health status, tracking of expenditures and outputs for improving efficiency of investments are hallmarks of successful health programs. In recent times, public health intelligence platforms, such as the WHO’s Epidemic Intelligence from open sources (EIOS), utilize strong data systems facilitated by digital technologies for health emergency preparedness and disease surveillance. Innovative digital technologies including mHealth have potential to offer new insights and tools to improve clinical decision making, data security and predictive analytics. Realizing the potential of mHealth to achieve development goals will require collaboratively addressing multiple challenges, including strengthening underlying digital infrastructure and digital health systems, working to improve data quality, responsible management and sharing of patient data, and eventually trust, security and utilization of data to inform strategic planning of health interventions. Thus, it is recommended that African health sector leaderships convene roundtable discussions to discuss critical policy dimensions of strengthening mHealth ecosystems, and lay the foundation for responsibly developing and adopting new innovations like mHealth-facilitated Artificial Intelligence (AI) applications in addressing privacy related issues. Such discussions should include but not limited to discussions on adopting latest advances in mHealth technologies including AI tools and telemedicine techniques in advancing population health. They should identify concrete actions for shaping policy and enabling environments to foster mHealth technologies for accelerated improvements in health and related development programs; showcase AI-driven innovative solutions for health, and share best practices from countries, including possibilities for customizations. Such approach could foster a deeper interest on the use of mHealth technologies to strengthen service delivery, improve the collection of quality data and promote data protection rights among African economies.
Exploratory spatial data analyses identified positive spatial autocorrelation for the periods evaluated, as well as varying cluster patterns of TB treatment completion rates across the periods of study evaluation. There was a direct spatial relationship between TB treatment completion rates and mobile phone use among related African countries. Spatial autocorrelation patterns generated were consistent with Low-Low and High-Low cluster patterns and were significant at different p-values. Algeria and Senegal had significant clusters across the study periods, while DRC, Niger, South Africa, and Cameroon had significant clusters in at least two time-periods. ESDA identified statistically significant associations between TB treatment completion rates and mobile phone use. Countries with higher rates of mobile phone use, showed higher TB treatment completion rates overall, indicating enhanced program uptake. Thus, there is need to strengthen national policies that promote TB medication adherence and completion using mHealth strategies among African health systems. African government should identify turnaround strategies to strengthen mHealth technologies and improve health outcomes.
African countries used in this analysis as listed by the World Health Organization. Available at: http://www.who.int/countries/en/ accessed April 2, 2020.
Algeria, Burundi, Burkina Faso, Benin, Angola, Cameroon, Botswana, Cape Verde, Central African Republic, Comoros, Chad, Congo, Democratic Republic of Congo, Côte d’Ivoire, Djibouti, Equatorial Guinea, Egypt, Eritrea, Ethiopia, Gabon, Ghana, Guinea-Bissau, Lesotho, Gambia, Guinea, Kenya, Liberia, Libya, Malawi, Mauritania, Mali, Madagascar, Mauritius, Mozambique, Morocco, Nigeria, Namibia, Niger, Sao Tome and Principe, Seychelles, Rwanda, Senegal, Sierra Leone, Somalia, South Africa, South Sudan, Sudan, Swaziland, Togo, Uganda, Tunisia, Tanzania, Zambia, Zimbabwe.
Variables | Moran’s I value | Pseudo p-value | |
---|---|---|---|
TB_TreatmentCompletionRate_Yr2000 | 0.0190 | 0.021 | |
Univariate Global Moran’s I | TB_TreatmentCompletionRate_Yr2005 | 0.0177 | 0.032 |
TB_TreatmentCompletionRate_Yr2010 | 0.0196 | 0.025 | |
TB_TreatmentCompletionRate_Yr2015 | 0.0179 | 0.031 |
SI, NU and JO conceived, coordinated, and wrote the first draft of the manuscript. JO and FZ participated in the study conception and overall study coordination. NK, JO and FZ contributed to writing the subsequent drafts of the manuscript. SI, NU and JO did the final review and edit of the draft manuscript. All authors read and approved the final draft manuscript before publication. All authors contributed to the article and approved the submitted version.
The authors declare that they have no competing interests.
The dataset generated and/or analyzed during the current study are available in the World Bank database [http://data.worldbank.org/]; the International Telecommunication Union database [http://www.itu.int/en/ITU-D/Statistics/Pages/stat/default.aspx]; and the World Health Organization repository [http://www.who.int/countries/en/].
SMS | Short Message Services |
TB | Tuberculosis |
WHO | World Health Organization |
mHealth | Mobile Health |
ICT | Information and Communication Technology |
ESDA | Exploratory Spatial Data Analytic |
LISA | Local Indicator of Spatial Association |
LDMI | Local Differential Moran’s I. |
Heavy metal pollution is an environmental problem that has harmful effect on both aquatic and terrestrial environment. These metals are released to the environment through activities such as mining, electroplating and manufacturing of paper and pesticides in form of mine tailings or effluents [1]. They have ability to complex with minerals to form inorganic ligands with variable solubility and acid–base potentials, thus, making their remediation from contaminated land/soil a major concern [2, 3].
Pollution arising from heavy metals poses serious health problems to both human beings and animals [1].
Clay minerals and metal oxides are formed from weathering of primary minerals [24]. These minerals have high surface area and can absorb heavy metals from aqueous and natural environments [25]. Clay minerals, bentonite, sepiolite and palygorskite have been used extensively to remove heavy metals from wastewater and agricultural soil, and the mechanisms of remediation are sorption, precipitation and liming [26]. Heavy metal polluted water is mostly remediated using ion-exchange, adsorption and mechanism [27]. Even though, clay minerals have adsorption affinity for heavy metals, e.g. Cu and Zn, their roles are not significant when compared to iron oxides (e.g. goethite), manganese oxides (e.g. birnessite) and organic materials on a unit mass basis [28]. Comparison of the adsorption potentials of deep sea minerals such as clay minerals, Mn-oxides, Fe-oxides, calcite and apatite reveal that Mn and Fe oxides and oxyhydroxides are crucial phases for scavenging heavy metals [29] Lead readily sorbs on all phases but has greatest affinity for carbonate fluorapatite, however, Caesium (Cs) has affinity for illite [29]. In sea water, hydrated cations such as Mn2+, Co2+, Ni2+, Zn2+, Cu2+, Ba2+, MnCl+ and PbCl+ have strong affinity for Mn-oxide while HVO42−, MoO42−, PbCO3 and HAsO42− preferentially adsorb onto Fe oxyhydroxide [29].
Sorption techniques have the ability to remove these contaminants via adsorption onto sorbents. However, the type of sorbent to be used for remediation depends on the sorption capacity, sorption pH and distribution coefficient of the contaminant [30]. The review on the sorption of Ni(II) adsorbents indicates that bisorbents are the most effective for removal of the ion from aqueous solution [31]. In addition, Pb and Cd be successfully immobilised with wide range of low cost materials such as metal oxides, animal manure, apatite, lime, biosolids, and biochar [32]. However, the review on the adsorption capabilities of low-cost sorbents such as agricultural waste, household wastes, industrial by-products and sludge indicates that even though these material has great adsorption potentials their particle size, surface area, contact time, initial concentration of ion, adoption dose are not stated by the researchers [33]. This poses great limitation for the use of these adsorbents for remediation. Further review of the sorption of nickel, copper, lead, cadmium, caesium, chromium, europium and thorium on both natural and synthetic materials reveal that more studies on multi-component sorption of these metals are required [34]. Therefore, synthetizing effective and low cost adsorbent that can be recycled for removal of contaminants from aqueous environment will be of high interest [34]. Similarly, synthesising and discovering new novel methods of using modified clay for environmental remediation is required metals [25].
To this end, this paper presents the review the sorption of heavy metals such as Ni, Co, Cu, Zn, V, Pb, Hg, In, As, Cd, Cr, Ga, Cs, Mn, Eu, Mo, Th, TI and Cr on both natural and synthetic metal oxides and clay minerals for soil and water remediation. The main aim of this review is to summarise the adsorption mechanism and recent remediation method of single and multicomponent system of these toxic metals using clay minerals and metal oxides. In addition, the advantages of reusability these adsorbents after remediation are discussed.
The interactions between metallic ions and mineral surfaces in any environment allow the sorption of ions to the solid surface, thereby decreasing the concentration of ions in the aqueous phases below the solubility limits of the solid phase [35]. Determination of partitioning of heavy metals among the solid phase and accurately predicting their mobility in natural environment requires adequate knowledge of the chemical process such as ion exchange, adsorption, surface precipitation, coprecipitation and mineralisation, that govern sorption mechanism [36]. For example, cobalt sorbs to goethite through surface complexation, surface precipitate and structural incorporation depending on the concentration and sorption duration [37].
Surfaces of substances (oxides, organic and inorganic) have surface functional groups or hydroxyl groups of solute ligands [38]. These functional groups are dominant in natural environments as oxides of Al, Fe and Si and in aqueous solution. The surface charge of metallic oxy-hydroxides, phosphate and carbonates is formed through ionisation of surface groups [39]. The pH of surface oxide and oxy-hydroxides changes due to adsorption of protons or ions from solution [40]. Thus, the surface charge set up potential differences between the sorbent and sorbate, thereby influencing the approach of ions towards the surfaces [40]. Consequently, surface hydroxyl groups are responsible for complexation on metal oxides, oxyhydroxides, hydroxides and aluminosilicates. The type of surface functional group influences the sequence of the adsorption reaction, variation in adsorption solution chemistry, electrical properties of the interface and the adsorption ability [41]. The reaction of metals and oxygen atoms at the surface results in the formation of hydroxyl groups (OH−), which are taken as part of the surface instead of solution. The surface hydroxyl is amphoteric (i.e. they can either accept a proton or donate a proton) as shown below:
Adsorption of metal to the surface takes place via substitution of surface protons (H+) to form inner sphere complexes:
The surface oxygen, ΞSO− may attract ions from bulk solution to form outer sphere complexes [42]:
Bidentate ligands (Lewis bases, e.g. Cl−, OH−, H2O, NH3+) are sorbed to the surface by the replacement of the surface hydroxyl group (ΞSOH) as follows:
Adsorbed ligands can also take up another metal while metals already adsorbed can attach themselves to another ligand [43].
An adsorption isotherm is a relationship between the amount adsorbed and the concentration of the adsorbate at a constant temperature [39]. Both empirical and chemical models are used in describing the adsorption reaction. The former model uses mathematical expressions to interpret adsorption (e.g. Freundlich isotherm, Langmuir isotherm and distribution coefficient) whereas the latter uses a molecular approach to calculate equilibrium constants (e.g. constant capacitance model, triple layer models) [44]. Langmuir isotherm is based on the assumption that only one monolayer is formed during reaction, presence of equivalent sites, immobility of adsorbate and absence of adsorbate-adsorbent interaction [39]. The difference between Langmuir isotherm and Freundlich is that Langmuir isotherm considers maximum sorption whereas Freundlich considers infinity site [39]. However, adsorption isotherms are of limited application when modelling because of the complex and variability of natural environment with heavy metal and existence of sorbents with pH dependent surface charges [39]. Therefore, application of surface complexation models that can integrate both the experimental data and the electrostatic interaction between the ion and the oxide surface is required for modelling the mobility sorption of heavy metal. Computer models such as MINTEQ, FITEQL EQLFOR, HYDRAQL and SOILCHEM can calculate both equilibrium speciation and constants [44, 45, 46].
Adsorption kinetic model is used to investigate sorption mechanism as well as the rate controlling steps in a batch reaction [34]. Kinetic studies is carried out in a way to vary the initial concentration of adsorbate, temperature, time, sorbent dosage, particle size, pH, type of sorbent and sorbate [34]. It is a continuous measurement of experimental data until equilibrium is attained. The result is tested using kinetic equations to determine the best fit, which will give a better understanding of the sorption mechanism. The adsorption isotherms and kinetics commonly used are listed in Table 1. In addition, most of the adsorption of ions on clays and oxides are best described by Langmuir, Dubinin-Radushkevich and Freundlich isotherm models and Pseudo-second-order kinetic model [47, 48, 49, 50, 51, 52, 53].
Isotherm equations | Kinetic equations |
---|---|
Brunauer, Emmett and Teller (BET) | |
Adsorption isotherm and kinetic model equations.
θ = fraction of surface coverage; [M] = concentration of ion; Ce = concentration at equilibrium; Cs = solubility of adsorbate at a particular temperature; qmax = saturated monolayer sorption capacity; qe = the amount of solute adsorbed at equilibrium; q = the amount of solute adsorbed at any given time ‘t’ #; C = the concentrations of sorbate in solution at any given time ‘t’; Cs = the concentrations of sorbate in sorbent at any time ‘t’.
Better understanding of sorption mechanism is done using technologies and spectroscopy studies such as Attenuated Total Reflection Infrared [37, 54], Fourier Transform Infrared (FTIR) spectroscopy, extend X-ray absorption fine structure spectroscopy (EXAFS) [55, 56, 57], powder X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and Electron paramagnetic resonance (EPR) [58]. Spectroscopic studies show that copper, nickel, zinc and cobalt bind to Mn(IV) vacancy sites in birnessite to form inner-sphere surface complexes via interlayer triple-corner-sharing or enter the vacancy site to become part of the structure [56]. ATR-FTIR is very useful in distinguishing the outer-sphere and inner-sphere complexes on minerals. Yoon et al., determined of the types and structures of the adsorption complexes formed by oxalate at boehmite (γ-AlOOH)/water and corundum (α-Al2O3)/water interfaces using in situ ATR-FTIR spectroscopy and quantum chemical [54]. Their findings suggest that the adsorption mechanism involves loss of protons from aqueous species during ligand-exchange reaction and is useful clue on the transport mechanism and removal of toxic elements in natural water.
Clay minerals, e.g. montmorillonite, illite, and kaolinite, are known to have ability of adsorbing heavy metals in their inter layers through ion exchange reaction [25]. They generally have high sorption and expansion properties and are widely used for removal of contaminants from aqueous solution [25]. Their specific roles for adsorption of heavy metals from aqueous solutions and natural environments are discussed below. These adsorbents and the metals they are capable of removing from aqueous solution are summarised in Table 2.
Metals | Adsorbents | Temperature (°C) | Concentration | Optimum recovery pH | Time for maximum adsorption | References |
---|---|---|---|---|---|---|
Zn(II) Cu(II) Mn(II) Cd(II) Pb(II) Ni(II) | Montmorillonite | 25–26.85 | 500 mg/L | 6–8 | 180 min | [47, 62, 63] |
U(VI) Th(IV) | Jordanian Bentonite | 25 | 100 mg/L | 3 | 18 h | [49] |
Cu(II) Ag(I) | Verde-lodo bentonite | Cu: 60 Ag: 20 | 1.2429 mmol/L | <4.5 | 2 days | [75] |
Th(IV) In(II) | Activated bentonite Chitosan-coated bentonite | 25 | 70 mg/L | 4.0 | 300 min | [76] [77] |
Cs(II) | Mixture of iron pillared Layered montmorillonite (80%) and goethite (20%) | 15 | 13.3 mg/L | 7.3. | 30 min | [50] |
Cu(II) Cs(II) | Aluminium-pillared-layered montmorillonites | — | 100 mg/L | For Cu 4.0–6.0 and For Cs 3.0–8.0 | 1.5 h | [51] |
Cr(VI)) | Magnetite nanoparticles | 25 | 50 mg/L | 3.0 | 3 h | [53] |
Mn(II) Ni(II) Cu(II) | Hexagonal birnessite | 25 | 143 mg/L | 7–8 | 24 h– 22 days | [55] [100] |
Pb(II) Cu(II) Zn(II) Cd(II) | Hexagonal birnessite Hydrous Mn-oxide (HMO)-coated clay | 25 | 2801 mg/L | 4.5 to ∼5.5 | 24 h– 2 weeks | [101] [102] |
Hg(II) Cr(III) Pb(II) Cu(II) Zn(II) Ba(II) Ni(II) Mn(II) Cd(II) Ba(II) Ag(I) | Ca-montmorillonite | — | 1 N | 4.8 | 16 h | [64] |
Eu(III) | Na-montmorillonite | 25 | 1 × 10−3 mol/L | ∼ 7 | 8 days | [65] |
Cd(II) | Heated ball clay Combination of montmorillonite and humic acid | 30 | 50 mg/L | 8 8.5 | 18 h 24 h | [68] [111] [112] |
Pb(II) Cd(II) Ni(II) Cu(II) | Kaolinite | 30 | 160 mg/L | 7 | 30 min | [69] |
Cd(II) Co(II) Cu(II) Pb(II) Ni(II) Cr(VI) | Acid-activated form kaolinite | 30 | 250 mg/L | Co and Ni: pH 7.8 Cu and Pb: Ph 5.8 Cd: Ph 10, Cr: pH 7 | 40–240 min | [70] [71] |
Cs(II) | Clay soil with predominantly illite as clay mineral | 25 | 4 mg/L | 8 | 16 h | [72] [73] |
TI(I) | Illite | 25 | 8.39 × 10−6 mol/L | 7.18 | 6 days | [74] |
Pb(II) Cu(II) Ni(II) | Synthetic magnesium-aluminium layered double hydroxides modified palygorskite | 18–40 | 500 mg/L | 5.0 | 4.0, 8.0, and 20.0 min, for Pb(II), Cu(II) and Ni(II), respectively | [84] |
Pb(II) | Palygorskite-iron oxide nanocomposite | 25 | 12 h | [85] | ||
As(III) Cd(II) Cr(III) Cu(II) Hg(II) Ni(II) Pb(II) | Fe-oxide modified smectites (montmorillonite and saponite) | 25 | 100 μg/L | pH 5 | 2 h | [88] |
Ga(III) V(V) Co(II) Ni(II) | Goethite | 20–25 | 10–58 mg/L | pH 7 | 24 h | [38] [93] [94] [98] |
Cu(II) Zn(II) Cd(II) Pb(II) | Amine-magnetic Fe-oxide | 30 | 1.0 mmol/L | 6 | 60 min | [103] |
Ni(II) | Mixture of goethite, humic acid and kaolinite | 30 | 100 mg/L | 5.5 | 2 h | [104] |
Summary of metals, potential adsorbents and experimental parameters.
The sorption ability of montmorillonite and its remediation potential for nickel and copper from polluted water was investigated by [47]. In their study, sorption rate follows pseudo-second-order rate model and the adsorption model fits to Langmuir model. Also, the point of zero charge (PZC) for the aqueous solution containing both metal at different ionic strengths 0.01 and 0.001 M KCl, is pH 3.4 ± 0.2 [47]. In contrast, the sorption of cadmium, chromium and lead (II) from wastewater on clay follow 1st order kinetics and can be modelled with both Freundlich and Langmuir model [59]. This study reveals that clay has the capability of removing these metals from aqueous solution at low temperature. In another study, the adsorption of Pb on clay from Tunisia reached maximum at pH 7 and declined above pH 7 due to formation of Pb precipitates, and the mechanism of adsorption via ion exchange [60]. Similarly, sorption of Cu(II) and Ni(II) onto white montmorillonite from obtained Kahramanmaras show increased adsorption with increasing amount of the initial amount of adsorbent, pH and temperature. The white montmorillonite shows more affinity for Cu(II) with 100% adsorption compared to Ni(II) [61]. In another study, sorption of Ni(II) on montmorillonite is influence by the presence of copper in a bi-metal aqueous solution with distortion of the shape of the adsorption isotherm whereas the presence of nickel has negligible effect on the sorption of copper [58]. EPR and XAS analyses of adsorption data reveal that both copper form inner-sphere complexes at pH 8 in both single-metal and binary metal system. However, nickel in single metal system forms inner-sphere complex at pH 8 but in binary-solute systems, it forms Ni phyllosilicate co-precipitate/alpha-Ni(OH)2(s) precipitate at pH 8.0 [58]. In another study, the sorption of Ni(II) and Mn(II) on montmorillonite from Ugwuoba, Nigeria, reveals 90% removal of these ions from solution containing 500 mg/L at pH 6.0 with maximum adsorption capacity of 166.67 mg/g for nickel and 142.86 mg/g for manganese [62]. Acid treated montmorillonite has enhance adsorption ability for heavy metals (Zn, Cu, Mn, Cd, Pb, Ni), depending on the initial metal concentration [63].
Similarly, the adsorption of mercury, chromium, lead, copper, zinc, barium, nickel, manganese, cadmium, silver on Ca-montmorillonite from single metal solutions followed second-order at greater rate compared to montmorillonite [64]. Copper, lead and chromium forms surface precipitation with montmorillonite whereas mercury, zinc, barium, nickel manganese, cadmium and silver sorb onto montmorillonite via adsorption and ion exchange to form both inner and outer sphere complex at the silanol and aluminol site [64]. However, sorption of bi-metal solution of these metals is better described with Langmuir isotherm model [64]. In another study, Europium (III) sorbs on Na-montmorillonite to form an outer-sphere complex at the exchange site as well as inner-sphere surface complexes at the ‘aluminol’ and ‘silanol’ edge sites [65]. In another study, heavy metals such as Hg(II), Cr(III), Pb(II), Cu(II), Zn(II), Ba(II), Ni(II), Mn(II), Cd(II), Ba(II) and Ag(I) in a single metal system adsorbs more on Ca-montmorillonite compared to Na-montmorillonite [66]. The adsorption selective sequence is Hg(II) > Zn(II) > Ba(II) > Cd(II) > Ni(II) > Mn(II). However, Na-Montmorillonite is more effective for removal of Pb(II), Cu(II), Co(II), Cd(II) and Zn(II) from aqueous solution than Ca-Montmorillonite [66]. In general, montmorillonite clay and its modified form has stronger adsorption capacity for arsenic, cadmium, chromium, cobalt, lead, iron, manganese, nickel and zinc than kaolinite and its modified form [67].
Adsorption of Cd, Cu, Ni, Zn, Pb and Cr with Ball clay (kaolinite with high plasticity) at 30°C indicates that it sorbs more ion compared to Ca-montmorillonite, illite, kaolinite and Kaolin, and has the higher affinity for cd relative to other metals [68]. The sorption was at the maximum at pH 6 and 100% adsorption of 50 mg/L Cd. The sorption rate follows pseudo-first-order kinetics whereas the Langmuir model is used to describe the isotherm model [68]. Similarly, Pb(II), Cd(II), Ni(II) and Cu(II) sorption on kaolinitic clay from Longyan, China, show maximum sorption in 30 min and reduction of Pb concentration from 160.00 to 8.00 mg/L [69]. Another study found that adsorption of Cd(II), Co(II), Cu(II), Pb(II) and Ni(II) onto Acid treated kaolinite have great potential for removal these metals from aqueous solution compared to untreated kaolinite [70]. However, the use of natural and modified kaolinite clays for the removal of Cr(VI) for contaminated water is pH dependent and the adsorption increases from pH 1–2 at equilibration time of 240 min [71].
The adsorption of Caesium on clay made up of predominately of illite in the presence of small amount of organic matter and Fe-Oxide indicate that presence of organic matter play significant role for Cs uptake. The adsorption is described by Freundlich [48]. Maximum sorption of Caesium on to clay soil occurs at pH 8 and ambient temperature [72]. Comparative study of Cs sorption on illite, montmorillonite and kaolinite show that Cs is most reactive and has strong affinity for illite compared to other clay [73]. The sorption data was successfully modelled with 1-pK Diffuse layer model [73]. In another study, thallium is found to associate with illite in natural environment and sorption studies reveal that TI(I) sorbs more onto illite than smectite [74]. The affinity for TI follows this sequence: MnO2 > illite > smectite = ferrihydrite > = Al2O3 = goethite > SiO2. However, in presence of Rb, Cs, Ti adsorption to illite is less [74].
Removal of silver and copper in a binary solution containing the two ions with Verde-lodo bentonite reveals that the adsorbent has high adsorption affinity for copper than silver [75]. Cu adsorption on Verde-lodo bentonite is more at an elevated temperature and attained adsorption capacity of 0.110 mmol/g at 60°C, whereas silver attained 0.090 mmol/g at 20°C [75]. In another study, adsorption of indium on chitosan-coated bentonite is best described by Langmuir isotherm whereas the adsorption kinetics fits the pseudo second order [76]. Thorium (IV) sorption onto activated bentonite depends on temperature, pH, ionic strength, and type of anion and the adsorption kinetics can be described by pseudo-second-order model [77]. The activated bentonite is effective for removal of thorium (IV) and associates with it via surface complexation [77]. In the another study, bentonite was effectively used to remove thorium (IV) at pH 3, equilibration time of 18 h and 25°C and adsorption was fitted to Freundlich, Langmuir and Dubinin-Radushkevich isotherm models. Desorption experiment shows that thorium (IV) is best recovered with 1.0 M HNO3 [49]. However, the use of bentonite for sorption of heavy metals has some negative effect. This is because increase in concentration of heavy metals such as zinc, lead and copper results to decrease in liquid limit, swelling potential, swelling pressure and free swelling of bentonite but increases its hydraulic conductivity due to sorption of heavy metal in the double layer structure [78].
Competitive adsorption and desorption cadmium, chromium, copper, lead and zinc on natural clay show difference in the optimum maximum pH of adsorption and metal affinity for single and multi-element adsorption [79]. The adsorption sequence for single metal sorption is Cr > Pb > Cu > Cd > Zn whereas Cr > Cu > Pb > Cd > Zn is the obtained sequence in the multicomponent system. The study also notes that the initial pH determines the solubility and removal of heavy metal in competitive multi element scenario [79]. In both the single and multielement adsorption, about 90–100% metal uptake expect Zn was achieved at pH 2–12 [79]. In another study, sorption of Cd, Cu, Pb, and Zn with concentration of 10 mmol/L on clay minerals, Fe rich clay minerals, clay-Fe oxide, Fe-oxyhydroxides, and calcite at both alkaline and acidic condition show that cadmium and zinc are adsorbed in acidic media by clay minerals whereas copper and lead sorb more at alkaline meda [80]. Sorption of Pb(II), Cd(II), Cu(II) and Zn(II) on clay obtained from Aleg formation, Tunisia that has surface area of 71 m2/g indicate adsorption sequence of Pb(II) > Cu(II) > Zn(II) > Cd(II) and capacity of 131.58 mg/g in single metal systems and less than 50.10 mg/g for multi-metal [81]. Another study found that Cd(II) adsorption is effective for clay samples heated at 200°C, however, above 200°C adsorption decreases as a result of loss of SiOH or Al–OH binding sites [68]. Similarly, clay from china shows to be effective for removal of Cd at 30°C [82]. In addition, investigation for the temperature and pH effect on Cr(VI) adsorption reveal that sorption rate increases with increasing temperature and decreasing pH for concentration range of 0.743–1.422 mg/g [83].
Synthetic magnesium-aluminium layered double hydroxides modified palygorskite shows high adsorption capacity for of Pb(II), Cu(II) and Ni(II) in the aqueous solution with initial concentration of 100 mg/L at pH 5.0 [84]. The reaction fit into Langmuir isotherm and the pseudo-second-order kinetic model [84]. In another study, the use of synthetic palygorskite-Fe oxide nanocomposite removal of Pb(II) from aqueous solution with initial 20–500 mg/L Pb indicates that the adsorbent has maximum Pb(II) adsorption capacity of 26.6 mg/g at 5 g/L adsorbent 150 min−1 stirring speed, and 25°C [85]. The adsorption data best fitted to the Langmuir isotherm model and pseudo-second-order kinetic model [85].
Montmorillonite clay modified with tetramethylammonium cations show enhances adsorption capacity for copper compared with unmodified montmorillonite, and removed up to 99.4% Cu(II) from aqueous solution with adsorption capacity of 925.93 mg/g [86]. Another study found that modification of clay minerals with hexadecylammonium bromide (HDTMA) is effective for attenuation of As(III) and As(V) in the presence of Cd(II), Cu(II) and Mn(II) and anions such as glycine, iminodiacetic acid, ethylenediaminetetraacetic acid disodium salt, oxalic acid, phosphate and sulfate [87]. In contrast, Fe-oxide modified smectites (montmorillonite and saponite) have the best adsorption capacity for removal of As(III), Cd(II), Cr(III), Cu(II), Hg(II), Ni(II), Pb(II) and Zn(II) from aqueous solution with at concentration of 10–100 ppb [88]. Mercury is sequestered in Al pillared Clay from Aleg formation, Tunisia at pH 3.2 and 240 min equilibration time [89]. The adsorption fit to Langmuir model with adsorption capacities 49.75 mg/g whereas the adsorption kinetics fits to pseudo-second-order kinetic. The adsorption reaction is exothermic [89]. Another study found that Indium sorbs readily on montmorillonite Metosol modified with di(2-ethylhexyl) phosphoric acid with kinetics that follow pseudo-first- and pseudo-second-order models [89]. Sorption of copper and caesium on Al-pillared montmorillonites follow a pseudo-first-order equation and pH of sorption 4.0–6.0 for copper and 3.0–8.0 for caesium [51]. Caesium sorption is best described with Langmuir model while copper fits the Freundlich isotherm model [51]. Sorption of Cs onto Fe-pillared montmorillonite, goethite and their mixture show that optimum sorption pH range is 5–9 and 93% removal of Cs occurred with the mixture of 20% goethite with Fe-pillared montmorillonite. The sorption process is exothermic and follows pseudo-first-order kinetics and can be described with Dubinin-Radushkevich, Freundlich and Langmuir models [50]. Also, combination of Al-pillared montmorillonite and Fe3O4 an MMT/Fe3O4 removes Cs from contaminated soil and water and can be recycled efficiently, and can be applied for the remediation of Cs contaminated land. The adsorption follow pseudo-second-order kinetics and Freundlich isotherm model [52]. In addition, maximum adsorption of Cr(IV) from aqueous solution was achieved by using clay heated at 200 to 400°C [91]. The heating process increased the exposure of the adsorptive site and the adsorptive capabilities [91].
The Fe3+ oxides and Mn-oxides such as goethite, magnetite and birnessite are usually used in sorption studies of heavy metals and anions because of its simple synthesis in the laboratory [40, 92]. These metal oxides act as hosts for toxic trace elements with valences of +2, +3 and +5 [92]. The potential use of these minerals and their mixtures for remediation of contaminated land are reviewed below.
Gallium adsorbs on to goethite to form Ga hexa-coordinated >FeOGa (OH)(2)(0) surface complexes at both acid and alkaline pH and exhibit the same isotope fractionation [93]. In another study, vanadium (V) adsorbs onto goethite to form bidentate corner-sharing complex from initial solution of 2.5 and 25 mg/L at pH 1.5 to 12 [94]. Mononuclear V(V) complexes are present at 25 ppm whereas both mononuclear and polynuclear V(V) complexes exist at 25 mg//solution species form [94]. In another study, at concentration < 10 mg/L and pH 7, cobalt sorbs on goethite at pH 7 to form bidentate edge and corner complexes but form surface precipitates, bidentate edge and corner complexes from 10 to 58 mg/L and pH 7.5 [37]. With ageing, Co sorption on goethite is irreversible depending on the initial concentration [37]. In addition, sorption of Pb, Hg, Cd, Zn, Cu, Ni, Co, Mn, Cr and Al on goethite from solution 10−6 M was achieved in 2 h and 20°C, but different pH [94]. The pH of 50% sorbed metals (pH 50) ranges from 2.81 for Hg to 6.45 for Mn [95]. The adsorption of Cu(II) with initial concentration of 25 mg/L onto goethite, haematite and lepidocrocite from pH 2–7 reveal that at pH of total metal sorption is 6 for goethite, 6.2 for haematite and 6.8 for lepidocrocite [56]. In same study, EXAFS spectra show that Cu(II) adsorbs these Fe-(hydr)oxides to form two or three bidentate edge sharing, corner sharing and tridentate complexes [56]. Adsorption of Ni, Zn, and Ca onto the goethite reveal that goethite has stronger affinity for Ni and Zn compared to Ca, however, in no observable competition occur in Ni–Ca and Zn–Ca bi-metal systems [96]. The adsorption is well described with single-site Langmuir model [96]. In another study, indium with concentration of 6–29 μg/L was immobilised form acid mine drainage by raising it pH to 8 and subsequent sorption onto iron oxide [97]. In addition, up to 100 mg/L Ni sorbs onto goethite at pH 8, 25°C and equilibration time of 21 days [98].
Mn(II) forms edge-sharing complex with birnessite whereas Ni(II) forms triple corner-sharing complexes at pH 6.5–7.5, however, the addition of Mn(II) in Ni(II)-birnessite suspension at pH 6.5 results to formation of edge-sharing Ni(II) complexes due to site competition [99]. However, at pH 7.5, the presence of Mn(II) results to transformation of birnessite into feitknechtite that encourages sorption and incorporation of Ni(II) from solution [99]. This suggests that alteration of birnessite can influence the solubility of nickel in anaerobic environment [98]. In another study, hexagonal birnessite (δ-MnO2) was used to sorb Cu(II) containing 143, 77 and 32 mg/L at pH 1–9 [100]. At pH 3, 100% adsorption results to about 5, 2.5 and 1% of copper in the adsorbate [100]. However, EXFAS characterisation of adsorbates at pH 4 reveals that Cu forms by inner-sphere complexation whereas at pH 8, it associates with birnessite via structurally incorporation [100]. Sorption of Zn onto synthetic δ-MnO2 from an initial solution containing 2000 mg/L of Zn occurs at pH ∼ 1 and at maximum pH ∼5 [101]. However, desorption reaction indicates the Zn sorption is reversible and EXFAS show that it form inner-sphere surface complexes at high pH [101]. Similarly, removal of Pb from solution containing 810, 1782, 2801 mg/L occur at pH ∼5.5 pH and equilibration time of 2 weeks, thus indication high sorption capacity of birnessite for Pb [101]. Also, desorption experiment show that the sorption is reversible at pH ∼1 [101]. In another study, sorption of Pb(II), Cu(II), Zn(II), Cd(II) onto hexagonal birnessite was carried out at pH 4.5 and characterised with powder X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). The result of the study indicates that sorption capacity of biressinte for these metals follow this sequence: Pb2+ ≫ Cu2+ > Zn2+ > Cd2+ but Pb sorption is up to 3.9 times more than other metals [102].
Synthetic magnetite nano particles was used to remove Hexavalent chromium (Cr(VI)) from synthetic wastewater containing 0 to 50 mg/L Cr(IV) at pH 3.0 and 30°C.Up to 72% of Cr was removed via adsorption and the isotherm fitted to Freundlich model [53]. In addition, rapid sorption of Cu(II), Zn(II), Cd(II), Pb(II) and Ni(II) on synthetic Amine-magnetic Fe-oxide is influenced by pH, ionic strength and the complexation of amino groups [101]. Maximum adsorption occur at pH 6, ionic strength of 1.0 mmol/L NaCl and duration of 60 min and are best described with Pseudo-second-order kinetic model, Langmuir model [101]. The adsorption affinity of the adsorbent follow this sequence Pb(II) > Cu(II) > Zn(II) > Cd(II) > Ni(II) [103].
Mixture of goethite, humic acid and kaolinite are good adsorbents for lead, cadmium, zinc, nickel and copper and the adsorption is better described with Langmuir and Freundlich isotherm model [104]. However, in a five metal ion system (Quinary), the adsorption of lead, cadmium and nickel are affected negatively by the presence of zinc and copper whereas the presence of lead, cadmium and nickel has synergistic effect on the sorption of zinc and copper [104]. Another study found that low-cost adsorbent Algeria clay that is composed of predominantly montmorillonite and kaolinite has the capacity of adsorbing Cu(II) at pH of 6.5 and 20°C with maximum adsorption capacity of 12.22 mg/g [105]. However, treated Algeria clay under similar condition as the untreated clay has adsorption capacity of 15.40 mg/g [105]. The process of adsorption was spontaneous and exothermic [105]. Sorption of copper (II) ion on palygorskite and sepiolite is enhanced at elevated temperature [106]. The adsorption reactions are endothermically driven but sepiolite sorbs copper spontaneously and has more copper retention capacity compared to palygorskite [106]. In another study, combination of montmorillonite and ZnO show high capacity for adsorption of Pb and Cu from aqueous solution at wide range of pH [107]. The kinetic of the adsorption reaction follow pseudo-second-order whereas the adsorption isotherm is described by Langmuir isotherm [107]. Arsenic adsorption on goethite, amorphous Fe-hydroxide, and Ti(IV)-Fe(III)-Al(III)-pillared bentonite, clay pillared with titanium (IV), iron (III), and aluminium (III) reveal that amorphous Fe-hydroxide has highest adsorption capacity for arsenate and arsenite [108]. Arsenic is stable at pH 7 and is mobilised at pH 4 and 10 but mostly at acidic condition. Mn- oxides, amorphous iron oxides and clay minerals sequester up to 61% of arsenic [109].
Combination of montmorillonite and humic acid in the ratio of 100:3 is efficient for removal of cadmium at pH 8.5 and contact time of 24 h with adsorption capacity of 18.96 mg/g for cadmium [110]. Another study reveal that the adsorption and desorption of cadmium and copper from montmorillonite, allophane, kaolinite, halloysite reveal that sericite has the highest ability for Cd sorption, however, montmorillonite showed greatest retention for Cd [111]. In addition, all clay types has sorption ability for copper with pH of 50% metal sorbed lower than pH of 50% metal sorbed for cadmium sorption [111]. In another study, the removal of Cu and Zn from aqueous solution by Al-montmorillonite, goethite, kaolinite and their mixtures at room temperature and pH 4 reveal that adsorption is via inner and outer sphere complexation [112]. However, mixing of different mineral for sorption of Cu and Zn retards their removal and decreases the exchange of proton and acid/base potential of the reactive sites [112]. The sorption of Zn onto hydrous Mn-oxide (HMO)-coated clay reveals that the affinity the HMO-coated montmorillonite was greater than that of uncoated montmorillonite, and possess linear isotherm at pH 5–6 [113]. X-ray absorption spectroscopy (XAS) reveal reduction of first shell distance at surface loading of 10−3 mol and pH 5–7 due to higher electrostatic attraction [113]. In another study, sorption of copper, zinc and lead on soil composed of clay minerals (smectites and vermiculites), carbonates and Fe-oxide show that Copper and lead has higher sorption capacity and retention compared to Zn [114]. Clay minerals adsorbs more metals than other phases, however, for lead, similar capacity was obtained for Fe-oxides [114]. The presence of carbonate in alkaline condition increases the amount of metal uptake, and the mixture of clay minerals and Fe-oxide enhanced adsorption of the metals [114]. Competitive sorption and desorption of Cd, Cr, Cu, Ni, Pb and Zn by iron oxide, Mn oxides, kaolinite, vermiculite and mica from initial solution of 100 mg/L show that kaolinite and mica has strong affinity and retention capability for cd; vermiculite, Cu and Zn; iron oxide and Mn-oxide, Pb [115]. Kaolinite has low retention capability for Cu whereas vermiculite and Mn oxide has greatest retention capability of all the metal [115].
In another study, the effect of increase surface area of clay minerals (kaolinite, montmorillonite and illite) through coating with Fe-oxide, organic matter and Al-oxides for adsorption of heavy metals indicate that coating clay increases the surface area of clay minerals with expectation of Aluminium oxide coated montmorillonite and organic matter coated 2:1 phyllosilicates [116]. Another study found that, both amorphous hydrous manganese oxide (HMO) and HMO-coated montmorillonite sorbs Ni and Pb to form inner-sphere complexes with Ni coordinating to vacant site of Mn-oxide structure and Pb forming bidentate corner-sharing complexes [117]. In addition, another study reveal that montmorillonite clay coated with amorphous (hydrous manganese oxide (HMO), birnessite and pyrolusite has the same surface properties as the coated oxide, however, the surface area of the coated Montmorillonite increases whereas the while the pore size distribution decreased. The HMO- and birnessite-coated clay still retained their pH (point of net zero charge (pnzc)) of 2.8 and 3.1, respectively, [118].
The use of clay minerals and oxides is more effective than using other materials for remediation of heavy metals from the environment. From example, the use of sepioloite is better for remediation of Cd compared to Ca(OH)2 [119]. In addition, clay minerals and oxides can be recycled and regenerated for additional remediation use. For example, synthetic palygorskite-Fe oxide exhibited the capability of removing Pb and three cycles reusable potential and retains it magnetic properties for the removal of the heavy metals [85]. Recovery of metals from sorbents can increase the life cycle and long term remediation cost [120]. The estimated zinc that will accumulate in composite substrate in Force Crag Mine is will amount to €7600 in 10 years, however, removal of this substrate after its exhaustion will cost more than €0.8 M whereas recycling the substrate through acid washing is estimated to cost €155,000 [120]. Similarly, oxides and clay minerals can be recycled and reused for remediation of the contaminant. In addition, these sorbents can be used to remediate economic heavy/rare earth metals for commercial and industrial purposes, however, this requires further investigation.
Oxides and clay minerals have large surface areas and can sorb heavy metals via adsorption and ion exchange, respectively. Sorption of these toxic metals on oxides and clay minerals reduce their concentration and mobility in aqueous solution and natural environment. This review confirms that sorption is highly dependent on pH, equilibration time, initial concentration of adsorbate, type of adsorbent, temperature, type of adsorbent modification and surface area. In addition, most of the adsorption of ions on clays and oxides are best described by Langmuir models and Pseudo-second-order model. Most remediation techniques employ the use of permeable reactive barriers (PBRs) to react the contaminant from groundwater. These barriers can be Fe-oxides, montmorillonite, Mn oxide-coated montmorillonite, Fe-oxide-coated montmorillonite [121]. The review confirmed that both metal oxides and clay have capability of sequestering heavy metals, however, combination of both metal oxides and modified clay have enhanced capability of removing heavy metals from aqueous solution. These inorganic adsorbents has the regeneration and recycling potentials and can be used to remediate and sequester economic metals for commercial purposes, however, this needs future investigation.
IntechOpen publishes different types of publications
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They are considered as the biotechnologically valuable bacteria that are exploited for its secondary metabolite production. Approximately, 10,000 bioactive metabolites are produced by Actinobacteria, which is 45% of all bioactive microbial metabolites discovered. Especially Streptomyces species produce industrially important microorganisms as they are a rich source of several useful bioactive natural products with potential applications. Though it has various applications, some Actinobacteria have its own negative effect against plants, animals, and humans. On this context, this chapter summarizes the general characteristics of Actinobacteria, its habitat, systematic classification, various biotechnological applications, and negative impact on plants and animals.",book:{id:"5056",slug:"actinobacteria-basics-and-biotechnological-applications",title:"Actinobacteria",fullTitle:"Actinobacteria - Basics and Biotechnological Applications"},signatures:"Ranjani Anandan, Dhanasekaran Dharumadurai and Gopinath\nPonnusamy Manogaran",authors:[{id:"48914",title:"Dr.",name:"Dharumadurai",middleName:null,surname:"Dhanasekaran",slug:"dharumadurai-dhanasekaran",fullName:"Dharumadurai Dhanasekaran"}]},{id:"37734",doi:"10.5772/46006",title:"Endosomal Escape Pathways for Non-Viral Nucleic Acid Delivery Systems",slug:"endosomal-escape-pathways-for-non-viral-nucleic-acid-delivery-systems",totalDownloads:7388,totalCrossrefCites:33,totalDimensionsCites:91,abstract:null,book:{id:"2617",slug:"molecular-regulation-of-endocytosis",title:"Molecular Regulation of Endocytosis",fullTitle:"Molecular Regulation of Endocytosis"},signatures:"Wanling Liang and Jenny K. 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They are considered as the biotechnologically valuable bacteria that are exploited for its secondary metabolite production. Approximately, 10,000 bioactive metabolites are produced by Actinobacteria, which is 45% of all bioactive microbial metabolites discovered. Especially Streptomyces species produce industrially important microorganisms as they are a rich source of several useful bioactive natural products with potential applications. Though it has various applications, some Actinobacteria have its own negative effect against plants, animals, and humans. On this context, this chapter summarizes the general characteristics of Actinobacteria, its habitat, systematic classification, various biotechnological applications, and negative impact on plants and animals.",book:{id:"5056",slug:"actinobacteria-basics-and-biotechnological-applications",title:"Actinobacteria",fullTitle:"Actinobacteria - Basics and Biotechnological Applications"},signatures:"Ranjani Anandan, Dhanasekaran Dharumadurai and Gopinath\nPonnusamy Manogaran",authors:[{id:"48914",title:"Dr.",name:"Dharumadurai",middleName:null,surname:"Dhanasekaran",slug:"dharumadurai-dhanasekaran",fullName:"Dharumadurai Dhanasekaran"}]},{id:"35104",title:"Restriction Fragment Length Polymorphism Analysis of PCR-Amplified Fragments (PCR-RFLP) and Gel Electrophoresis - Valuable Tool for Genotyping and Genetic Fingerprinting",slug:"restriction-fragment-length-polymorphism-analysis-of-pcr-amplified-fragments-pcr-rflp-and-related-te",totalDownloads:34054,totalCrossrefCites:6,totalDimensionsCites:26,abstract:null,book:{id:"1770",slug:"gel-electrophoresis-principles-and-basics",title:"Gel Electrophoresis",fullTitle:"Gel Electrophoresis - Principles and Basics"},signatures:"Henrik Berg Rasmussen",authors:[{id:"114068",title:"Dr.",name:"Henrik",middleName:null,surname:"Rasmussen",slug:"henrik-rasmussen",fullName:"Henrik Rasmussen"}]},{id:"50471",title:"Molecular Mechanisms of Skin Aging and Rejuvenation",slug:"molecular-mechanisms-of-skin-aging-and-rejuvenation",totalDownloads:5110,totalCrossrefCites:6,totalDimensionsCites:13,abstract:"The aging process in the skin is complex and influenced by more intrinsic and extrinsic factors than any other body organ. The effects of these two types of factors overlap for the most part. The combined effects of these two aging processes also affect dermal matrix alterations. The main clinical signs of skin aging include wrinkling and irregular pigmentation, which are influenced by a combination of intrinsic and extrinsic (e.g., UV radiation, heat, smoking, and pollutants) factors. Histologically, collagen decreases, and the dermis is replaced by abnormal elastic fibers as a cause of wrinkle formation through the loss of skin elasticity. There have been numerous studies of skin aging performed to elucidate the underlying molecular mechanisms and to develop various antiaging therapeutics and preventive strategies. We summarized the molecular mechanisms and treatments of skin aging. Mainly UV radiation induces ROS formation and DNA damage, leading to increased production of MMPs and decreased production of collagen in keratinocytes and fibroblasts, which reflect the central aspects of skin aging. Besides UV radiation exposure, extrinsic factors including tobacco smoking, exposure to environmental pollutants, infrared radiation, and heat contribute to premature skin aging. Like UV radiation, these factors cause ROS formation and increase expression of MMPs, thus accelerating skin aging by inducing extracellular matrix (ECM) degradation. Accumulated collagen fibrils inhibit the new collagen synthesis and account for the further degradation of the ECM through this positive feedback loop. Accumulating evidence for molecular mechanisms of skin aging should provide clinicians with an expanding spectrum of therapeutic targets in the treatment of skin aging.",book:{id:"5258",slug:"molecular-mechanisms-of-the-aging-process-and-rejuvenation",title:"Molecular Mechanisms of the Aging Process and Rejuvenation",fullTitle:"Molecular Mechanisms of the Aging Process and Rejuvenation"},signatures:"Miri Kim and Hyun Jeong Park",authors:[{id:"47695",title:"Prof.",name:"Hyun Jeong",middleName:null,surname:"Park",slug:"hyun-jeong-park",fullName:"Hyun Jeong Park"},{id:"185767",title:"Prof.",name:"Miri",middleName:null,surname:"Kim",slug:"miri-kim",fullName:"Miri Kim"}]},{id:"62731",title:"An Introductory Chapter: Secondary Metabolites",slug:"an-introductory-chapter-secondary-metabolites",totalDownloads:9738,totalCrossrefCites:33,totalDimensionsCites:52,abstract:null,book:{id:"6670",slug:"secondary-metabolites-sources-and-applications",title:"Secondary Metabolites",fullTitle:"Secondary Metabolites - Sources and Applications"},signatures:"Durairaj Thirumurugan, Alagappan Cholarajan, Suresh S.S. 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Prior to his appointment at Stellenbosch University, he has been at the University of Pretoria, Department of Computer Science (1998-2018), where he was appointed as South Africa Research Chair in Artifical Intelligence (2007-2018), the head of the Department of Computer Science (2008-2017), and Director of the Institute for Big Data and Data Science (2017-2018). 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He is a full professor of signal processing and pattern recognition and is head of the Signals and Communications Department at ULPGC, teaching from 2001 on subjects on signal processing and learning theory. His research lines are biometrics, biomedical signals and images, data mining, classification system, signal and image processing, machine learning, and environmental intelligence. He has researched in 52 international and Spanish research projects, some of them as head researcher. He is co-author of 4 books, co-editor of 27 proceedings books, guest editor for 8 JCR-ISI international journals, and up to 24 book chapters. He has over 450 papers published in international journals and conferences (81 of them indexed on JCR – ISI - Web of Science). He has published seven patents in the Spanish Patent and Trademark Office. He has been a supervisor on 8 Ph.D. theses (11 more are under supervision), and 130 master theses. He is the founder of The IEEE IWOBI conference series and the president of its Steering Committee, as well as the founder of both the InnoEducaTIC and APPIS conference series. He is an evaluator of project proposals for the European Union (H2020), Medical Research Council (MRC, UK), Spanish Government (ANECA, Spain), Research National Agency (ANR, France), DAAD (Germany), Argentinian Government, and the Colombian Institutions. He has been a reviewer in different indexed international journals (<70) and conferences (<250) since 2001. He has been a member of the IASTED Technical Committee on Image Processing from 2007 and a member of the IASTED Technical Committee on Artificial Intelligence and Expert Systems from 2011. \n\nHe has held the general chair position for the following: ACM-APPIS (2020, 2021), IEEE-IWOBI (2019, 2020 and 2020), A PPIS (2018, 2019), IEEE-IWOBI (2014, 2015, 2017, 2018), InnoEducaTIC (2014, 2017), IEEE-INES (2013), NoLISP (2011), JRBP (2012), and IEEE-ICCST (2005)\n\nHe is an associate editor of the Computational Intelligence and Neuroscience Journal (Hindawi – Q2 JCR-ISI). He was vice dean from 2004 to 2010 in the Higher Technical School of Telecommunication Engineers at ULPGC and the vice dean of Graduate and Postgraduate Studies from March 2013 to November 2017. He won the “Catedra Telefonica” Awards in Modality of Knowledge Transfer, 2017, 2018, and 2019 editions, and awards in Modality of COVID Research in 2020.\n\nPublic References:\nResearcher ID http://www.researcherid.com/rid/N-5967-2014\nORCID https://orcid.org/0000-0002-4621-2768 \nScopus Author ID https://www.scopus.com/authid/detail.uri?authorId=6602376272\nScholar Google https://scholar.google.es/citations?user=G1ks9nIAAAAJ&hl=en \nResearchGate https://www.researchgate.net/profile/Carlos_Travieso",institutionString:null,institution:{name:"University of Las Palmas de Gran Canaria",institutionURL:null,country:{name:"Spain"}}},editorTwo:null,editorThree:null},{id:"23",title:"Computational Neuroscience",coverUrl:"https://cdn.intechopen.com/series_topics/covers/23.jpg",isOpenForSubmission:!0,editor:{id:"14004",title:"Dr.",name:"Magnus",middleName:null,surname:"Johnsson",slug:"magnus-johnsson",fullName:"Magnus Johnsson",profilePictureURL:"https://mts.intechopen.com/storage/users/14004/images/system/14004.png",biography:"Dr Magnus Johnsson is a cross-disciplinary scientist, lecturer, scientific editor and AI/machine learning consultant from Sweden. \n\nHe is currently at Malmö University in Sweden, but also held positions at Lund University in Sweden and at Moscow Engineering Physics Institute. \nHe holds editorial positions at several international scientific journals and has served as a scientific editor for books and special journal issues. \nHis research interests are wide and include, but are not limited to, autonomous systems, computer modeling, artificial neural networks, artificial intelligence, cognitive neuroscience, cognitive robotics, cognitive architectures, cognitive aids and the philosophy of mind. \n\nDr. Johnsson has experience from working in the industry and he has a keen interest in the application of neural networks and artificial intelligence to fields like industry, finance, and medicine. \n\nWeb page: www.magnusjohnsson.se",institutionString:null,institution:{name:"Malmö University",institutionURL:null,country:{name:"Sweden"}}},editorTwo:null,editorThree:null},{id:"24",title:"Computer Vision",coverUrl:"https://cdn.intechopen.com/series_topics/covers/24.jpg",isOpenForSubmission:!0,editor:{id:"294154",title:"Prof.",name:"George",middleName:null,surname:"Papakostas",slug:"george-papakostas",fullName:"George Papakostas",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002hYaGbQAK/Profile_Picture_1624519712088",biography:"George A. Papakostas has received a diploma in Electrical and Computer Engineering in 1999 and the M.Sc. and Ph.D. degrees in Electrical and Computer Engineering in 2002 and 2007, respectively, from the Democritus University of Thrace (DUTH), Greece. Dr. Papakostas serves as a Tenured Full Professor at the Department of Computer Science, International Hellenic University, Greece. Dr. Papakostas has 10 years of experience in large-scale systems design as a senior software engineer and technical manager, and 20 years of research experience in the field of Artificial Intelligence. Currently, he is the Head of the “Visual Computing” division of HUman-MAchines INteraction Laboratory (HUMAIN-Lab) and the Director of the MPhil program “Advanced Technologies in Informatics and Computers” hosted by the Department of Computer Science, International Hellenic University. He has (co)authored more than 150 publications in indexed journals, international conferences and book chapters, 1 book (in Greek), 3 edited books, and 5 journal special issues. His publications have more than 2100 citations with h-index 27 (GoogleScholar). His research interests include computer/machine vision, machine learning, pattern recognition, computational intelligence. \nDr. Papakostas served as a reviewer in numerous journals, as a program\ncommittee member in international conferences and he is a member of the IAENG, MIR Labs, EUCogIII, INSTICC and the Technical Chamber of Greece (TEE).",institutionString:null,institution:{name:"International Hellenic University",institutionURL:null,country:{name:"Greece"}}},editorTwo:null,editorThree:null},{id:"25",title:"Evolutionary Computation",coverUrl:"https://cdn.intechopen.com/series_topics/covers/25.jpg",isOpenForSubmission:!0,editor:{id:"136112",title:"Dr.",name:"Sebastian",middleName:null,surname:"Ventura Soto",slug:"sebastian-ventura-soto",fullName:"Sebastian Ventura Soto",profilePictureURL:"https://mts.intechopen.com/storage/users/136112/images/system/136112.png",biography:"Sebastian Ventura is a Spanish researcher, a full professor with the Department of Computer Science and Numerical Analysis, University of Córdoba. Dr Ventura also holds the positions of Affiliated Professor at Virginia Commonwealth University (Richmond, USA) and Distinguished Adjunct Professor at King Abdulaziz University (Jeddah, Saudi Arabia). Additionally, he is deputy director of the Andalusian Research Institute in Data Science and Computational Intelligence (DaSCI) and heads the Knowledge Discovery and Intelligent Systems Research Laboratory. He has published more than ten books and over 300 articles in journals and scientific conferences. Currently, his work has received over 18,000 citations according to Google Scholar, including more than 2200 citations in 2020. In the last five years, he has published more than 60 papers in international journals indexed in the JCR (around 70% of them belonging to first quartile journals) and he has edited some Springer books “Supervised Descriptive Pattern Mining” (2018), “Multiple Instance Learning - Foundations and Algorithms” (2016), and “Pattern Mining with Evolutionary Algorithms” (2016). He has also been involved in more than 20 research projects supported by the Spanish and Andalusian governments and the European Union. He currently belongs to the editorial board of PeerJ Computer Science, Information Fusion and Engineering Applications of Artificial Intelligence journals, being also associate editor of Applied Computational Intelligence and Soft Computing and IEEE Transactions on Cybernetics. Finally, he is editor-in-chief of Progress in Artificial Intelligence. He is a Senior Member of the IEEE Computer, the IEEE Computational Intelligence, and the IEEE Systems, Man, and Cybernetics Societies, and the Association of Computing Machinery (ACM). Finally, his main research interests include data science, computational intelligence, and their applications.",institutionString:null,institution:{name:"University of Córdoba",institutionURL:null,country:{name:"Spain"}}},editorTwo:null,editorThree:null},{id:"26",title:"Machine Learning and Data Mining",coverUrl:"https://cdn.intechopen.com/series_topics/covers/26.jpg",isOpenForSubmission:!0,editor:{id:"24555",title:"Dr.",name:"Marco Antonio",middleName:null,surname:"Aceves Fernandez",slug:"marco-antonio-aceves-fernandez",fullName:"Marco Antonio Aceves Fernandez",profilePictureURL:"https://mts.intechopen.com/storage/users/24555/images/system/24555.jpg",biography:"Dr. Marco Antonio Aceves Fernandez obtained his B.Sc. (Eng.) in Telematics from the Universidad de Colima, Mexico. He obtained both his M.Sc. and Ph.D. from the University of Liverpool, England, in the field of Intelligent Systems. He is a full professor at the Universidad Autonoma de Queretaro, Mexico, and a member of the National System of Researchers (SNI) since 2009. Dr. Aceves Fernandez has published more than 80 research papers as well as a number of book chapters and congress papers. He has contributed in more than 20 funded research projects, both academic and industrial, in the area of artificial intelligence, ranging from environmental, biomedical, automotive, aviation, consumer, and robotics to other applications. He is also a honorary president at the National Association of Embedded Systems (AMESE), a senior member of the IEEE, and a board member of many institutions. 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He is currently a principal researcher in data analytics and optimisation at TECNALIA (Spain), a visiting fellow at the Basque Center for Applied Mathematics (BCAM) and a part-time lecturer at the University of the Basque Country (UPV/EHU). His research interests gravitate on the use of descriptive, prescriptive and predictive algorithms for data mining and optimization in a diverse range of application fields such as Energy, Transport, Telecommunications, Health and Industry, among others. In these fields he has published more than 240 articles, co-supervised 8 Ph.D. theses, edited 6 books, coauthored 7 patents and participated/led more than 40 research projects. 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Buchholz and Erik J. Behringer",hash:"e373a3d1123dbd45fddf75d90e3e7c38",volumeInSeries:1,fullTitle:"Calcium and Signal Transduction",editors:[{id:"89438",title:"Dr.",name:"John N.",middleName:null,surname:"Buchholz",slug:"john-n.-buchholz",fullName:"John N. Buchholz",profilePictureURL:"https://mts.intechopen.com/storage/users/89438/images/6463_n.jpg",institutionString:null,institution:{name:"Loma Linda University",institutionURL:null,country:{name:"United States of America"}}}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null}]},subseriesFiltersForPublishedBooks:[{group:"subseries",caption:"Plant Physiology",value:13,count:1},{group:"subseries",caption:"Human Physiology",value:12,count:2},{group:"subseries",caption:"Cell Physiology",value:11,count:8}],publicationYearFilters:[{group:"publicationYear",caption:"2022",value:2022,count:1},{group:"publicationYear",caption:"2020",value:2020,count:4},{group:"publicationYear",caption:"2019",value:2019,count:5},{group:"publicationYear",caption:"2018",value:2018,count:1}],authors:{paginationCount:302,paginationItems:[{id:"198499",title:"Dr.",name:"Daniel",middleName:null,surname:"Glossman-Mitnik",slug:"daniel-glossman-mitnik",fullName:"Daniel Glossman-Mitnik",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/198499/images/system/198499.jpeg",biography:"Dr. Daniel Glossman-Mitnik is currently a Titular Researcher at the Centro de Investigación en Materiales Avanzados (CIMAV), Chihuahua, Mexico, as well as a National Researcher of Level III at the Consejo Nacional de Ciencia y Tecnología, Mexico. His research interest focuses on computational chemistry and molecular modeling of diverse systems of pharmacological, food, and alternative energy interests by resorting to DFT and Conceptual DFT. He has authored a coauthored more than 255 peer-reviewed papers, 32 book chapters, and 2 edited books. He has delivered speeches at many international and domestic conferences. He serves as a reviewer for more than eighty international journals, books, and research proposals as well as an editor for special issues of renowned scientific journals.",institutionString:"Centro de Investigación en Materiales Avanzados",institution:{name:"Centro de Investigación en Materiales Avanzados",country:{name:"Mexico"}}},{id:"76477",title:"Prof.",name:"Mirza",middleName:null,surname:"Hasanuzzaman",slug:"mirza-hasanuzzaman",fullName:"Mirza Hasanuzzaman",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/76477/images/system/76477.png",biography:"Dr. Mirza Hasanuzzaman is a Professor of Agronomy at Sher-e-Bangla Agricultural University, Bangladesh. He received his Ph.D. in Plant Stress Physiology and Antioxidant Metabolism from Ehime University, Japan, with a scholarship from the Japanese Government (MEXT). Later, he completed his postdoctoral research at the Center of Molecular Biosciences, University of the Ryukyus, Japan, as a recipient of the Japan Society for the Promotion of Science (JSPS) postdoctoral fellowship. He was also the recipient of the Australian Government Endeavour Research Fellowship for postdoctoral research as an adjunct senior researcher at the University of Tasmania, Australia. Dr. Hasanuzzaman’s current work is focused on the physiological and molecular mechanisms of environmental stress tolerance. Dr. Hasanuzzaman has published more than 150 articles in peer-reviewed journals. He has edited ten books and written more than forty book chapters on important aspects of plant physiology, plant stress tolerance, and crop production. According to Scopus, Dr. Hasanuzzaman’s publications have received more than 10,500 citations with an h-index of 53. He has been named a Highly Cited Researcher by Clarivate. He is an editor and reviewer for more than fifty peer-reviewed international journals and was a recipient of the “Publons Peer Review Award” in 2017, 2018, and 2019. He has been honored by different authorities for his outstanding performance in various fields like research and education, and he has received the World Academy of Science Young Scientist Award (2014) and the University Grants Commission (UGC) Award 2018. He is a fellow of the Bangladesh Academy of Sciences (BAS) and the Royal Society of Biology.",institutionString:"Sher-e-Bangla Agricultural University",institution:{name:"Sher-e-Bangla Agricultural University",country:{name:"Bangladesh"}}},{id:"187859",title:"Prof.",name:"Kusal",middleName:"K.",surname:"Das",slug:"kusal-das",fullName:"Kusal Das",position:null,profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bSBDeQAO/Profile_Picture_1623411145568",biography:"Kusal K. Das is a Distinguished Chair Professor of Physiology, Shri B. M. Patil Medical College and Director, Centre for Advanced Medical Research (CAMR), BLDE (Deemed to be University), Vijayapur, Karnataka, India. Dr. Das did his M.S. and Ph.D. in Human Physiology from the University of Calcutta, Kolkata. His area of research is focused on understanding of molecular mechanisms of heavy metal activated low oxygen sensing pathways in vascular pathophysiology. He has invented a new method of estimation of serum vitamin E. His expertise in critical experimental protocols on vascular functions in experimental animals was well documented by his quality of publications. He was a Visiting Professor of Medicine at University of Leeds, United Kingdom (2014-2016) and Tulane University, New Orleans, USA (2017). For his immense contribution in medical research Ministry of Science and Technology, Government of India conferred him 'G.P. Chatterjee Memorial Research Prize-2019” and he is also the recipient of 'Dr.Raja Ramanna State Scientist Award 2015” by Government of Karnataka. He is a Fellow of the Royal Society of Biology (FRSB), London and Honorary Fellow of Karnataka Science and Technology Academy, Department of Science and Technology, Government of Karnataka.",institutionString:"BLDE (Deemed to be University), India",institution:null},{id:"243660",title:"Dr.",name:"Mallanagouda Shivanagouda",middleName:null,surname:"Biradar",slug:"mallanagouda-shivanagouda-biradar",fullName:"Mallanagouda Shivanagouda Biradar",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/243660/images/system/243660.jpeg",biography:"M. S. Biradar is Vice Chancellor and Professor of Medicine of\nBLDE (Deemed to be University), Vijayapura, Karnataka, India.\nHe obtained his MD with a gold medal in General Medicine and\nhas devoted himself to medical teaching, research, and administrations. He has also immensely contributed to medical research\non vascular medicine, which is reflected by his numerous publications including books and book chapters. Professor Biradar was\nalso Visiting Professor at Tulane University School of Medicine, New Orleans, USA.",institutionString:"BLDE (Deemed to be University)",institution:{name:"BLDE University",country:{name:"India"}}},{id:"289796",title:"Dr.",name:"Swastika",middleName:null,surname:"Das",slug:"swastika-das",fullName:"Swastika Das",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/289796/images/system/289796.jpeg",biography:"Swastika N. Das is Professor of Chemistry at the V. P. Dr. P. G.\nHalakatti College of Engineering and Technology, BLDE (Deemed\nto be University), Vijayapura, Karnataka, India. She obtained an\nMSc, MPhil, and PhD in Chemistry from Sambalpur University,\nOdisha, India. Her areas of research interest are medicinal chemistry, chemical kinetics, and free radical chemistry. She is a member\nof the investigators who invented a new modified method of estimation of serum vitamin E. She has authored numerous publications including book\nchapters and is a mentor of doctoral curriculum at her university.",institutionString:"BLDEA’s V.P.Dr.P.G.Halakatti College of Engineering & Technology",institution:{name:"BLDE University",country:{name:"India"}}},{id:"248459",title:"Dr.",name:"Akikazu",middleName:null,surname:"Takada",slug:"akikazu-takada",fullName:"Akikazu Takada",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/248459/images/system/248459.png",biography:"Akikazu Takada was born in Japan, 1935. After graduation from\nKeio University School of Medicine and finishing his post-graduate studies, he worked at Roswell Park Memorial Institute NY,\nUSA. He then took a professorship at Hamamatsu University\nSchool of Medicine. In thrombosis studies, he found the SK\npotentiator that enhances plasminogen activation by streptokinase. He is very much interested in simultaneous measurements\nof fatty acids, amino acids, and tryptophan degradation products. By using fatty\nacid analyses, he indicated that plasma levels of trans-fatty acids of old men were\nfar higher in the US than Japanese men. . He also showed that eicosapentaenoic acid\n(EPA) and docosahexaenoic acid (DHA) levels are higher, and arachidonic acid\nlevels are lower in Japanese than US people. By using simultaneous LC/MS analyses\nof plasma levels of tryptophan metabolites, he recently found that plasma levels of\nserotonin, kynurenine, or 5-HIAA were higher in patients of mono- and bipolar\ndepression, which are significantly different from observations reported before. In\nview of recent reports that plasma tryptophan metabolites are mainly produced by\nmicrobiota. He is now working on the relationships between microbiota and depression or autism.",institutionString:"Hamamatsu University School of Medicine",institution:{name:"Hamamatsu University School of Medicine",country:{name:"Japan"}}},{id:"137240",title:"Prof.",name:"Mohammed",middleName:null,surname:"Khalid",slug:"mohammed-khalid",fullName:"Mohammed Khalid",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/137240/images/system/137240.png",biography:"Mohammed Khalid received his B.S. degree in chemistry in 2000 and Ph.D. degree in physical chemistry in 2007 from the University of Khartoum, Sudan. He moved to School of Chemistry, Faculty of Science, University of Sydney, Australia in 2009 and joined Dr. Ron Clarke as a postdoctoral fellow where he worked on the interaction of ATP with the phosphoenzyme of the Na+/K+-ATPase and dual mechanisms of allosteric acceleration of the Na+/K+-ATPase by ATP; then he went back to Department of Chemistry, University of Khartoum as an assistant professor, and in 2014 he was promoted as an associate professor. In 2011, he joined the staff of Department of Chemistry at Taif University, Saudi Arabia, where he is currently an assistant professor. His research interests include the following: P-Type ATPase enzyme kinetics and mechanisms, kinetics and mechanisms of redox reactions, autocatalytic reactions, computational enzyme kinetics, allosteric acceleration of P-type ATPases by ATP, exploring of allosteric sites of ATPases, and interaction of ATP with ATPases located in cell membranes.",institutionString:"Taif University",institution:{name:"Taif University",country:{name:"Saudi Arabia"}}},{id:"63810",title:"Prof.",name:"Jorge",middleName:null,surname:"Morales-Montor",slug:"jorge-morales-montor",fullName:"Jorge Morales-Montor",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/63810/images/system/63810.png",biography:"Dr. Jorge Morales-Montor was recognized with the Lola and Igo Flisser PUIS Award for best graduate thesis at the national level in the field of parasitology. He received a fellowship from the Fogarty Foundation to perform postdoctoral research stay at the University of Georgia. He has 153 journal articles to his credit. He has also edited several books and published more than fifty-five book chapters. He is a member of the Mexican Academy of Sciences, Latin American Academy of Sciences, and the National Academy of Medicine. He has received more than thirty-five awards and has supervised numerous bachelor’s, master’s, and Ph.D. students. Dr. Morales-Montor is the past president of the Mexican Society of Parasitology.",institutionString:"National Autonomous University of Mexico",institution:{name:"National Autonomous University of Mexico",country:{name:"Mexico"}}},{id:"217215",title:"Dr.",name:"Palash",middleName:null,surname:"Mandal",slug:"palash-mandal",fullName:"Palash Mandal",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/217215/images/system/217215.jpeg",biography:null,institutionString:"Charusat University",institution:null},{id:"49739",title:"Dr.",name:"Leszek",middleName:null,surname:"Szablewski",slug:"leszek-szablewski",fullName:"Leszek Szablewski",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/49739/images/system/49739.jpg",biography:"Leszek Szablewski is a professor of medical sciences. He received his M.S. in the Faculty of Biology from the University of Warsaw and his PhD degree from the Institute of Experimental Biology Polish Academy of Sciences. He habilitated in the Medical University of Warsaw, and he obtained his degree of Professor from the President of Poland. Professor Szablewski is the Head of Chair and Department of General Biology and Parasitology, Medical University of Warsaw. Professor Szablewski has published over 80 peer-reviewed papers in journals such as Journal of Alzheimer’s Disease, Biochim. Biophys. Acta Reviews of Cancer, Biol. Chem., J. Biomed. Sci., and Diabetes/Metabol. Res. Rev, Endocrine. He is the author of two books and four book chapters. He has edited four books, written 15 scripts for students, is the ad hoc reviewer of over 30 peer-reviewed journals, and editorial member of peer-reviewed journals. Prof. Szablewski’s research focuses on cell physiology, genetics, and pathophysiology. He works on the damage caused by lack of glucose homeostasis and changes in the expression and/or function of glucose transporters due to various diseases. He has given lectures, seminars, and exercises for students at the Medical University.",institutionString:"Medical University of Warsaw",institution:{name:"Medical University of Warsaw",country:{name:"Poland"}}},{id:"173123",title:"Dr.",name:"Maitham",middleName:null,surname:"Khajah",slug:"maitham-khajah",fullName:"Maitham Khajah",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/173123/images/system/173123.jpeg",biography:"Dr. Maitham A. Khajah received his degree in Pharmacy from Faculty of Pharmacy, Kuwait University, in 2003 and obtained his PhD degree in December 2009 from the University of Calgary, Canada (Gastrointestinal Science and Immunology). Since January 2010 he has been assistant professor in Kuwait University, Faculty of Pharmacy, Department of Pharmacology and Therapeutics. His research interest are molecular targets for the treatment of inflammatory bowel disease (IBD) and the mechanisms responsible for immune cell chemotaxis. He cosupervised many students for the MSc Molecular Biology Program, College of Graduate Studies, Kuwait University. Ever since joining Kuwait University in 2010, he got various grants as PI and Co-I. He was awarded the Best Young Researcher Award by Kuwait University, Research Sector, for the Year 2013–2014. He was a member in the organizing committee for three conferences organized by Kuwait University, Faculty of Pharmacy, as cochair and a member in the scientific committee (the 3rd, 4th, and 5th Kuwait International Pharmacy Conference).",institutionString:"Kuwait University",institution:{name:"Kuwait University",country:{name:"Kuwait"}}},{id:"195136",title:"Dr.",name:"Aya",middleName:null,surname:"Adel",slug:"aya-adel",fullName:"Aya Adel",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/195136/images/system/195136.jpg",biography:"Dr. Adel works as an Assistant Lecturer in the unit of Phoniatrics, Department of Otolaryngology, Ain Shams University in Cairo, Egypt. Dr. Adel is especially interested in joint attention and its impairment in autism spectrum disorder",institutionString:"Ain Shams University",institution:{name:"Ain Shams University",country:{name:"Egypt"}}},{id:"94911",title:"Dr.",name:"Boulenouar",middleName:null,surname:"Mesraoua",slug:"boulenouar-mesraoua",fullName:"Boulenouar Mesraoua",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/94911/images/system/94911.png",biography:"Dr Boulenouar Mesraoua is the Associate Professor of Clinical Neurology at Weill Cornell Medical College-Qatar and a Consultant Neurologist at Hamad Medical Corporation at the Neuroscience Department; He graduated as a Medical Doctor from the University of Oran, Algeria; he then moved to Belgium, the City of Liege, for a Residency in Internal Medicine and Neurology at Liege University; after getting the Belgian Board of Neurology (with high marks), he went to the National Hospital for Nervous Diseases, Queen Square, London, United Kingdom for a fellowship in Clinical Neurophysiology, under Pr Willison ; Dr Mesraoua had also further training in Epilepsy and Continuous EEG Monitoring for two years (from 2001-2003) in the Neurophysiology department of Zurich University, Switzerland, under late Pr Hans Gregor Wieser ,an internationally known epileptologist expert. \n\nDr B. Mesraoua is the Director of the Neurology Fellowship Program at the Neurology Section and an active member of the newly created Comprehensive Epilepsy Program at Hamad General Hospital, Doha, Qatar; he is also Assistant Director of the Residency Program at the Qatar Medical School. \nDr B. Mesraoua's main interests are Epilepsy, Multiple Sclerosis, and Clinical Neurology; He is the Chairman and the Organizer of the well known Qatar Epilepsy Symposium, he is running yearly for the past 14 years and which is considered a landmark in the Gulf region; He has also started last year , together with other epileptologists from Qatar, the region and elsewhere, a yearly International Epilepsy School Course, which was attended by many neurologists from the Area.\n\nInternationally, Dr Mesraoua is an active and elected member of the Commission on Eastern Mediterranean Region (EMR ) , a regional branch of the International League Against Epilepsy (ILAE), where he represents the Middle East and North Africa(MENA ) and where he holds the position of chief of the Epilepsy Epidemiology Section; Dr Mesraoua is a member of the American Academy of Neurology, the Europeen Academy of Neurology and the American Epilepsy Society.\n\nDr Mesraoua's main objectives are to encourage frequent gathering of the epileptologists/neurologists from the MENA region and the rest of the world, promote Epilepsy Teaching in the MENA Region, and encourage multicenter studies involving neurologists and epileptologists in the MENA region, particularly epilepsy epidemiological studies. \n\nDr. Mesraoua is the recipient of two research Grants, as the Lead Principal Investigator (750.000 USD and 250.000 USD) from the Qatar National Research Fund (QNRF) and the Hamad Hospital Internal Research Grant (IRGC), on the following topics : “Continuous EEG Monitoring in the ICU “ and on “Alpha-lactoalbumin , proof of concept in the treatment of epilepsy” .Dr Mesraoua is a reviewer for the journal \"seizures\" (Europeen Epilepsy Journal ) as well as dove journals ; Dr Mesraoua is the author and co-author of many peer reviewed publications and four book chapters in the field of Epilepsy and Clinical Neurology",institutionString:"Weill Cornell Medical College in Qatar",institution:{name:"Weill Cornell Medical College in Qatar",country:{name:"Qatar"}}},{id:"282429",title:"Prof.",name:"Covanis",middleName:null,surname:"Athanasios",slug:"covanis-athanasios",fullName:"Covanis Athanasios",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/282429/images/system/282429.jpg",biography:null,institutionString:"Neurology-Neurophysiology Department of the Children Hospital Agia Sophia",institution:null},{id:"190980",title:"Prof.",name:"Marwa",middleName:null,surname:"Mahmoud Saleh",slug:"marwa-mahmoud-saleh",fullName:"Marwa Mahmoud Saleh",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/190980/images/system/190980.jpg",biography:"Professor Marwa Mahmoud Saleh is a doctor of medicine and currently works in the unit of Phoniatrics, Department of Otolaryngology, Ain Shams University in Cairo, Egypt. She got her doctoral degree in 1991 and her doctoral thesis was accomplished in the University of Iowa, United States. Her publications covered a multitude of topics as videokymography, cochlear implants, stuttering, and dysphagia. She has lectured Egyptian phonology for many years. Her recent research interest is joint attention in autism.",institutionString:"Ain Shams University",institution:{name:"Ain Shams University",country:{name:"Egypt"}}},{id:"259190",title:"Dr.",name:"Syed Ali Raza",middleName:null,surname:"Naqvi",slug:"syed-ali-raza-naqvi",fullName:"Syed Ali Raza Naqvi",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/259190/images/system/259190.png",biography:"Dr. Naqvi is a radioanalytical chemist and is working as an associate professor of analytical chemistry in the Department of Chemistry, Government College University, Faisalabad, Pakistan. Advance separation techniques, nuclear analytical techniques and radiopharmaceutical analysis are the main courses that he is teaching to graduate and post-graduate students. In the research area, he is focusing on the development of organic- and biomolecule-based radiopharmaceuticals for diagnosis and therapy of infectious and cancerous diseases. Under the supervision of Dr. Naqvi, three students have completed their Ph.D. degrees and 41 students have completed their MS degrees. He has completed three research projects and is currently working on 2 projects entitled “Radiolabeling of fluoroquinolone derivatives for the diagnosis of deep-seated bacterial infections” and “Radiolabeled minigastrin peptides for diagnosis and therapy of NETs”. He has published about 100 research articles in international reputed journals and 7 book chapters. 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At the same time, they are faced with the Covid-19 pandemic leading to what some authors have called potential syndemics that might worsen the outcome of such infections. Therefore, it is important to conduct studies that examine parasitic infections in the context of the coronavirus pandemic for the benefit of all communities to help foster more informed decisions for the betterment of human and animal health.",coverUrl:"https://cdn.intechopen.com/series_topics/covers/5.jpg",keywords:"Blood Borne Parasites, Intestinal Parasites, Protozoa, Helminths, Arthropods, Water Born Parasites, Epidemiology, Molecular Biology, Systematics, Genomics, Proteomics, Ecology"},{id:"6",title:"Viral Infectious Diseases",scope:"The Viral Infectious Diseases Book Series aims to provide a comprehensive overview of recent research trends and discoveries in various viral infectious diseases emerging around the globe. The emergence of any viral disease is hard to anticipate, which often contributes to death. A viral disease can be defined as an infectious disease that has recently appeared within a population or exists in nature with the rapid expansion of incident or geographic range. This series will focus on various crucial factors related to emerging viral infectious diseases, including epidemiology, pathogenesis, host immune response, clinical manifestations, diagnosis, treatment, and clinical recommendations for managing viral infectious diseases, highlighting the recent issues with future directions for effective therapeutic strategies.",coverUrl:"https://cdn.intechopen.com/series_topics/covers/6.jpg",keywords:"Novel Viruses, Virus Transmission, Virus Evolution, Molecular Virology, Control and Prevention, Virus-host Interaction"}],annualVolumeBook:{},thematicCollection:[],selectedSeries:null,selectedSubseries:null},seriesLanding:{item:{id:"11",title:"Biochemistry",doi:"10.5772/intechopen.72877",issn:"2632-0983",scope:"Biochemistry, the study of chemical transformations occurring within living organisms, impacts all areas of life sciences, from molecular crystallography and genetics to ecology, medicine, and population biology. Biochemistry examines macromolecules - proteins, nucleic acids, carbohydrates, and lipids – and their building blocks, structures, functions, and interactions. Much of biochemistry is devoted to enzymes, proteins that catalyze chemical reactions, enzyme structures, mechanisms of action and their roles within cells. Biochemistry also studies small signaling molecules, coenzymes, inhibitors, vitamins, and hormones, which play roles in life processes. Biochemical experimentation, besides coopting classical chemistry methods, e.g., chromatography, adopted new techniques, e.g., X-ray diffraction, electron microscopy, NMR, radioisotopes, and developed sophisticated microbial genetic tools, e.g., auxotroph mutants and their revertants, fermentation, etc. More recently, biochemistry embraced the ‘big data’ omics systems. Initial biochemical studies have been exclusively analytic: dissecting, purifying, and examining individual components of a biological system; in the apt words of Efraim Racker (1913 –1991), “Don’t waste clean thinking on dirty enzymes.” Today, however, biochemistry is becoming more agglomerative and comprehensive, setting out to integrate and describe entirely particular biological systems. The ‘big data’ metabolomics can define the complement of small molecules, e.g., in a soil or biofilm sample; proteomics can distinguish all the comprising proteins, e.g., serum; metagenomics can identify all the genes in a complex environment, e.g., the bovine rumen. This Biochemistry Series will address the current research on biomolecules and the emerging trends with great promise.",coverUrl:"https://cdn.intechopen.com/series/covers/11.jpg",latestPublicationDate:"May 15th, 2022",hasOnlineFirst:!0,numberOfOpenTopics:4,numberOfPublishedChapters:286,numberOfPublishedBooks:27,editor:{id:"31610",title:"Dr.",name:"Miroslav",middleName:null,surname:"Blumenberg",fullName:"Miroslav Blumenberg",profilePictureURL:"https://mts.intechopen.com/storage/users/31610/images/system/31610.jpg",biography:"Miroslav Blumenberg, Ph.D., was born in Subotica and received his BSc in Belgrade, Yugoslavia. He completed his Ph.D. at MIT in Organic Chemistry; he followed up his Ph.D. with two postdoctoral study periods at Stanford University. Since 1983, he has been a faculty member of the RO Perelman Department of Dermatology, NYU School of Medicine, where he is codirector of a training grant in cutaneous biology. Dr. Blumenberg’s research is focused on the epidermis, expression of keratin genes, transcription profiling, keratinocyte differentiation, inflammatory diseases and cancers, and most recently the effects of the microbiome on the skin. He has published more than 100 peer-reviewed research articles and graduated numerous Ph.D. and postdoctoral students.",institutionString:null,institution:{name:"New York University Langone Medical Center",institutionURL:null,country:{name:"United States of America"}}},subseries:[{id:"14",title:"Cell and Molecular Biology",keywords:"Omics (Transcriptomics; Proteomics; Metabolomics), Molecular Biology, Cell Biology, Signal Transduction and Regulation, Cell Growth and Differentiation, Apoptosis, Necroptosis, Ferroptosis, Autophagy, Cell Cycle, Macromolecules and Complexes, Gene Expression",scope:"The Cell and Molecular Biology topic within the IntechOpen Biochemistry Series aims to rapidly publish contributions on all aspects of cell and molecular biology, including aspects related to biochemical and genetic research (not only in humans but all living beings). We encourage the submission of manuscripts that provide novel and mechanistic insights that report significant advances in the fields. Topics include, but are not limited to: Advanced techniques of cellular and molecular biology (Molecular methodologies, imaging techniques, and bioinformatics); Biological activities at the molecular level; Biological processes of cell functions, cell division, senescence, maintenance, and cell death; Biomolecules interactions; Cancer; Cell biology; Chemical biology; Computational biology; Cytochemistry; Developmental biology; Disease mechanisms and therapeutics; DNA, and RNA metabolism; Gene functions, genetics, and genomics; Genetics; Immunology; Medical microbiology; Molecular biology; Molecular genetics; Molecular processes of cell and organelle dynamics; Neuroscience; Protein biosynthesis, degradation, and functions; Regulation of molecular interactions in a cell; Signalling networks and system biology; Structural biology; Virology and microbiology.",annualVolume:11410,isOpenForSubmission:!0,coverUrl:"https://cdn.intechopen.com/series_topics/covers/14.jpg",editor:{id:"165627",title:"Dr.",name:"Rosa María",middleName:null,surname:"Martínez-Espinosa",fullName:"Rosa María Martínez-Espinosa",profilePictureURL:"https://mts.intechopen.com/storage/users/165627/images/system/165627.jpeg",institutionString:null,institution:{name:"University of Alicante",institutionURL:null,country:{name:"Spain"}}},editorTwo:null,editorThree:null,editorialBoard:[{id:"79367",title:"Dr.",name:"Ana Isabel",middleName:null,surname:"Flores",fullName:"Ana Isabel Flores",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRpIOQA0/Profile_Picture_1632418099564",institutionString:null,institution:{name:"Hospital Universitario 12 De Octubre",institutionURL:null,country:{name:"Spain"}}},{id:"328234",title:"Ph.D.",name:"Christian",middleName:null,surname:"Palavecino",fullName:"Christian Palavecino",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0033Y000030DhEhQAK/Profile_Picture_1628835318625",institutionString:null,institution:{name:"Central University of Chile",institutionURL:null,country:{name:"Chile"}}},{id:"186585",title:"Dr.",name:"Francisco Javier",middleName:null,surname:"Martin-Romero",fullName:"Francisco Javier Martin-Romero",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bSB3HQAW/Profile_Picture_1631258137641",institutionString:null,institution:{name:"University of Extremadura",institutionURL:null,country:{name:"Spain"}}}]},{id:"15",title:"Chemical Biology",keywords:"Phenolic Compounds, Essential Oils, Modification of Biomolecules, Glycobiology, Combinatorial Chemistry, Therapeutic peptides, Enzyme Inhibitors",scope:"Chemical biology spans the fields of chemistry and biology involving the application of biological and chemical molecules and techniques. In recent years, the application of chemistry to biological molecules has gained significant interest in medicinal and pharmacological studies. This topic will be devoted to understanding the interplay between biomolecules and chemical compounds, their structure and function, and their potential applications in related fields. Being a part of the biochemistry discipline, the ideas and concepts that have emerged from Chemical Biology have affected other related areas. This topic will closely deal with all emerging trends in this discipline.",annualVolume:11411,isOpenForSubmission:!0,coverUrl:"https://cdn.intechopen.com/series_topics/covers/15.jpg",editor:{id:"441442",title:"Dr.",name:"Şükrü",middleName:null,surname:"Beydemir",fullName:"Şükrü Beydemir",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0033Y00003GsUoIQAV/Profile_Picture_1634557147521",institutionString:null,institution:{name:"Anadolu University",institutionURL:null,country:{name:"Turkey"}}},editorTwo:{id:"13652",title:"Prof.",name:"Deniz",middleName:null,surname:"Ekinci",fullName:"Deniz Ekinci",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002aYLT1QAO/Profile_Picture_1634557223079",institutionString:null,institution:{name:"Ondokuz Mayıs University",institutionURL:null,country:{name:"Turkey"}}},editorThree:null,editorialBoard:[{id:"241413",title:"Dr.",name:"Azhar",middleName:null,surname:"Rasul",fullName:"Azhar Rasul",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRT1oQAG/Profile_Picture_1635251978933",institutionString:null,institution:{name:"Government College University, Faisalabad",institutionURL:null,country:{name:"Pakistan"}}},{id:"178316",title:"Ph.D.",name:"Sergey",middleName:null,surname:"Sedykh",fullName:"Sergey Sedykh",profilePictureURL:"https://mts.intechopen.com/storage/users/178316/images/system/178316.jfif",institutionString:null,institution:{name:"Novosibirsk State University",institutionURL:null,country:{name:"Russia"}}}]},{id:"17",title:"Metabolism",keywords:"Biomolecules Metabolism, Energy Metabolism, Metabolic Pathways, Key Metabolic Enzymes, Metabolic Adaptation",scope:"Metabolism is frequently defined in biochemistry textbooks as the overall process that allows living systems to acquire and use the free energy they need for their vital functions or the chemical processes that occur within a living organism to maintain life. Behind these definitions are hidden all the aspects of normal and pathological functioning of all processes that the topic ‘Metabolism’ will cover within the Biochemistry Series. Thus all studies on metabolism will be considered for publication.",annualVolume:11413,isOpenForSubmission:!0,coverUrl:"https://cdn.intechopen.com/series_topics/covers/17.jpg",editor:{id:"138626",title:"Dr.",name:"Yannis",middleName:null,surname:"Karamanos",fullName:"Yannis Karamanos",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002g6Jv2QAE/Profile_Picture_1629356660984",institutionString:null,institution:{name:"Artois University",institutionURL:null,country:{name:"France"}}},editorTwo:null,editorThree:null,editorialBoard:[{id:"243049",title:"Dr.",name:"Anca",middleName:null,surname:"Pantea Stoian",fullName:"Anca Pantea Stoian",profilePictureURL:"https://mts.intechopen.com/storage/users/243049/images/system/243049.jpg",institutionString:null,institution:{name:"Carol Davila University of Medicine and Pharmacy",institutionURL:null,country:{name:"Romania"}}},{id:"203824",title:"Dr.",name:"Attilio",middleName:null,surname:"Rigotti",fullName:"Attilio Rigotti",profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",institutionString:null,institution:{name:"Pontifical Catholic University of Chile",institutionURL:null,country:{name:"Chile"}}},{id:"300470",title:"Dr.",name:"Yanfei (Jacob)",middleName:null,surname:"Qi",fullName:"Yanfei (Jacob) Qi",profilePictureURL:"https://mts.intechopen.com/storage/users/300470/images/system/300470.jpg",institutionString:null,institution:{name:"Centenary Institute of Cancer Medicine and Cell Biology",institutionURL:null,country:{name:"Australia"}}}]},{id:"18",title:"Proteomics",keywords:"Mono- and Two-Dimensional Gel Electrophoresis (1-and 2-DE), Liquid Chromatography (LC), Mass Spectrometry/Tandem Mass Spectrometry (MS; MS/MS), Proteins",scope:"With the recognition that the human genome cannot provide answers to the etiology of a disorder, changes in the proteins expressed by a genome became a focus in research. Thus proteomics, an area of research that detects all protein forms expressed in an organism, including splice isoforms and post-translational modifications, is more suitable than genomics for a comprehensive understanding of the biochemical processes that govern life. The most common proteomics applications are currently in the clinical field for the identification, in a variety of biological matrices, of biomarkers for diagnosis and therapeutic intervention of disorders. From the comparison of proteomic profiles of control and disease or different physiological states, which may emerge, changes in protein expression can provide new insights into the roles played by some proteins in human pathologies. Understanding how proteins function and interact with each other is another goal of proteomics that makes this approach even more intriguing. Specialized technology and expertise are required to assess the proteome of any biological sample. Currently, proteomics relies mainly on mass spectrometry (MS) combined with electrophoretic (1 or 2-DE-MS) and/or chromatographic techniques (LC-MS/MS). MS is an excellent tool that has gained popularity in proteomics because of its ability to gather a complex body of information such as cataloging protein expression, identifying protein modification sites, and defining protein interactions. The Proteomics topic aims to attract contributions on all aspects of MS-based proteomics that, by pushing the boundaries of MS capabilities, may address biological problems that have not been resolved yet.",annualVolume:11414,isOpenForSubmission:!0,coverUrl:"https://cdn.intechopen.com/series_topics/covers/18.jpg",editor:{id:"200689",title:"Prof.",name:"Paolo",middleName:null,surname:"Iadarola",fullName:"Paolo Iadarola",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bSCl8QAG/Profile_Picture_1623568118342",institutionString:null,institution:{name:"University of Pavia",institutionURL:null,country:{name:"Italy"}}},editorTwo:{id:"201414",title:"Dr.",name:"Simona",middleName:null,surname:"Viglio",fullName:"Simona Viglio",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRKDHQA4/Profile_Picture_1630402531487",institutionString:null,institution:{name:"University of Pavia",institutionURL:null,country:{name:"Italy"}}},editorThree:null,editorialBoard:[{id:"72288",title:"Dr.",name:"Arli Aditya",middleName:null,surname:"Parikesit",fullName:"Arli Aditya Parikesit",profilePictureURL:"https://mts.intechopen.com/storage/users/72288/images/system/72288.jpg",institutionString:null,institution:{name:"Indonesia International Institute for Life Sciences",institutionURL:null,country:{name:"Indonesia"}}},{id:"40928",title:"Dr.",name:"Cesar",middleName:null,surname:"Lopez-Camarillo",fullName:"Cesar Lopez-Camarillo",profilePictureURL:"https://mts.intechopen.com/storage/users/40928/images/3884_n.png",institutionString:null,institution:{name:"Universidad Autónoma de la Ciudad de México",institutionURL:null,country:{name:"Mexico"}}},{id:"81926",title:"Dr.",name:"Shymaa",middleName:null,surname:"Enany",fullName:"Shymaa Enany",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRqB9QAK/Profile_Picture_1626163237970",institutionString:null,institution:{name:"Suez Canal University",institutionURL:null,country:{name:"Egypt"}}}]}]}},libraryRecommendation:{success:null,errors:{},institutions:[]},route:{name:"chapter.detail",path:"/chapters/77399",hash:"",query:{},params:{id:"77399"},fullPath:"/chapters/77399",meta:{},from:{name:null,path:"/",hash:"",query:{},params:{},fullPath:"/",meta:{}}}},function(){var e;(e=document.currentScript||document.scripts[document.scripts.length-1]).parentNode.removeChild(e)}()