Average values of aircraft engine emission factor recalculation into actual ambient temperature.
\\n\\n
Released this past November, the list is based on data collected from the Web of Science and highlights some of the world’s most influential scientific minds by naming the researchers whose publications over the previous decade have included a high number of Highly Cited Papers placing them among the top 1% most-cited.
\\n\\nWe wish to congratulate all of the researchers named and especially our authors on this amazing accomplishment! We are happy and proud to share in their success!
Note: Edited in March 2021
\\n"}]',published:!0,mainMedia:{caption:"Highly Cited",originalUrl:"/media/original/117"}},components:[{type:"htmlEditorComponent",content:'IntechOpen is proud to announce that 191 of our authors have made the Clarivate™ Highly Cited Researchers List for 2020, ranking them among the top 1% most-cited.
\n\nThroughout the years, the list has named a total of 261 IntechOpen authors as Highly Cited. Of those researchers, 69 have been featured on the list multiple times.
\n\n\n\nReleased this past November, the list is based on data collected from the Web of Science and highlights some of the world’s most influential scientific minds by naming the researchers whose publications over the previous decade have included a high number of Highly Cited Papers placing them among the top 1% most-cited.
\n\nWe wish to congratulate all of the researchers named and especially our authors on this amazing accomplishment! We are happy and proud to share in their success!
Note: Edited in March 2021
\n'}],latestNews:[{slug:"webinar-introduction-to-open-science-wednesday-18-may-1-pm-cest-20220518",title:"Webinar: Introduction to Open Science | Wednesday 18 May, 1 PM CEST"},{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"}]},book:{item:{type:"book",id:"7603",leadTitle:null,fullTitle:"Mixed Reality and Three-Dimensional Computer Graphics",title:"Mixed Reality and Three-Dimensional Computer Graphics",subtitle:null,reviewType:"peer-reviewed",abstract:"Mixed reality is an area of computer research that deals with the combination of real-world and computer-generated data, where computer-generated objects are visually mixed into the real environment and vice versa in real time. It is the newest virtual reality technology. It usually uses 3D computer graphics technologies for visual presentation of the virtual world. The mixed reality can be created using the following technologies: augmented reality and augmented virtuality. Mixed and virtual reality, their applications, 3D computer graphics and related technologies in their actual stage are the content of this book. 3D-modeling in virtual reality, a stereoscopy, and 3D solids reconstruction are presented in the first part. The second part contains examples of the applications of these technologies, in industrial, medical, and educational areas.",isbn:"978-1-83962-623-4",printIsbn:"978-1-83962-622-7",pdfIsbn:"978-1-83962-624-1",doi:"10.5772/intechopen.77405",price:119,priceEur:129,priceUsd:155,slug:"mixed-reality-and-three-dimensional-computer-graphics",numberOfPages:180,isOpenForSubmission:!1,isInWos:null,isInBkci:!1,hash:"96e6d4a84d98903e442415024f7403f5",bookSignature:"Branislav Sobota and Dragan Cvetković",publishedDate:"October 14th 2020",coverURL:"https://cdn.intechopen.com/books/images_new/7603.jpg",numberOfDownloads:7532,numberOfWosCitations:4,numberOfCrossrefCitations:11,numberOfCrossrefCitationsByBook:0,numberOfDimensionsCitations:18,numberOfDimensionsCitationsByBook:0,hasAltmetrics:1,numberOfTotalCitations:33,isAvailableForWebshopOrdering:!0,dateEndFirstStepPublish:"October 9th 2019",dateEndSecondStepPublish:"February 12th 2020",dateEndThirdStepPublish:"April 12th 2020",dateEndFourthStepPublish:"July 1st 2020",dateEndFifthStepPublish:"August 30th 2020",currentStepOfPublishingProcess:5,indexedIn:"1,2,3,4,5,6,7",editedByType:"Edited by",kuFlag:!1,featuredMarkup:null,editors:[{id:"109378",title:"Dr.",name:"Branislav",middleName:null,surname:"Sobota",slug:"branislav-sobota",fullName:"Branislav Sobota",profilePictureURL:"https://mts.intechopen.com/storage/users/109378/images/system/109378.jpeg",biography:"Branislav Sobota was born on 1967. In 1990, he graduated (MSc.) with honours at the Department of Computers and Informatics of the FEEI at Technical University in Košice. He defended his PhD. in 1999 and habilitation thesis in the field of virtual reality and computer graphics in 2008. He is working as an associate professor at the Department of Computers and Informatics Technical University of Kosice, Slovakia. His scientific research is focusing on computer graphics, parallel computing and especially virtual reality and related technologies.\n\nA researcher in virtual reality and related technologies, head of the LIRKIS DCI FEEI TU Košice (laboratory for research and development of new flexible and intelligent interfaces based on computer graphics and virtual reality technologies) and holder of 2 patents (Interactive school desk and Virtual control panel).",institutionString:"Technical University of Košice",position:null,outsideEditionCount:0,totalCites:0,totalAuthoredChapters:"3",totalChapterViews:"0",totalEditedBooks:"2",institution:{name:"Technical University of Košice",institutionURL:null,country:{name:"Slovakia"}}}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null,coeditorOne:{id:"101330",title:"Dr.",name:"Dragan",middleName:"Mladen",surname:"Cvetković",slug:"dragan-cvetkovic",fullName:"Dragan Cvetković",profilePictureURL:"https://mts.intechopen.com/storage/users/101330/images/system/101330.jpg",biography:"Dragan Cvetković obtained a Ph.D. in Aeronautics from the Faculty of Mechanical Engineering, University of Belgrade, in 1997. To date, he has published sixty-five books, scripts, and practicums about computers and computer programs, aviation weapons, and flight mechanics. He has published many scientific papers as well. Dr. Cvetković became a full professor of Informatics and Computing at Singidunum University, Belgrade, in 2014. Since 2019, he has been the vice-rector for teaching at the same university.",institutionString:"Singidunum University",position:null,outsideEditionCount:0,totalCites:0,totalAuthoredChapters:"4",totalChapterViews:"0",totalEditedBooks:"10",institution:{name:"Singidunum University",institutionURL:null,country:{name:"Serbia"}}},coeditorTwo:null,coeditorThree:null,coeditorFour:null,coeditorFive:null,topics:[{id:"572",title:"User Interface Design",slug:"user-interface-design"}],chapters:[{id:"70449",title:"Using Augmented Reality Technology to Construct a Wood Furniture Sampling Platform for Designers and Sample Makers to Narrow the Gap between Judgment and Prototype",doi:"10.5772/intechopen.90471",slug:"using-augmented-reality-technology-to-construct-a-wood-furniture-sampling-platform-for-designers-and",totalDownloads:807,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:0,abstract:"The production and design of wood furniture manufacturing includes manufacturing furniture parts and their assembly with appropriate finishing operations; the process requires repeated communication and discussions, as well as furniture sampling and trials, which are indispensable. However, in the sampling process, due to the different understandings of the designer and the sample maker in regard to the size of 2D drawings and the modeling of 3D furniture, the sampling results often differ greatly from the designer’s original concept; such errors appear mostly in the prototyping of wooden furniture. In this study, we focus on the wooden chair to explore whether augmented reality (AR) can contribute to the comparison between the virtual and physical shapes in the furniture prototyping process. We hope that by employing AR, the gap between the prototype and the finished furniture will be narrowed. By researching actual furniture prototyping with three furniture designers and two sample makers, this study has defined three furniture prototyping methods in the industry. Based on the basic principles, we recruited 38 designers to participate in the comparison experiments employing the above three different furniture prototypes. The results confirmed that applying the AR technology can effectively narrow the gap between judgment and prototype.",signatures:"I-Jui Lee",downloadPdfUrl:"/chapter/pdf-download/70449",previewPdfUrl:"/chapter/pdf-preview/70449",authors:[{id:"229636",title:"Dr.",name:"I-Jui",surname:"Lee",slug:"i-jui-lee",fullName:"I-Jui Lee"}],corrections:null},{id:"70925",title:"Augmented Reality as a New and Innovative Learning Platform for the Medical Area",doi:"10.5772/intechopen.90871",slug:"augmented-reality-as-a-new-and-innovative-learning-platform-for-the-medical-area",totalDownloads:643,totalCrossrefCites:1,totalDimensionsCites:1,hasAltmetrics:1,abstract:"This research paper shows an Augmented Reality (AR) project applied to medicine. The project is crystallized through a system, based on this new technology that serves as an innovative and innovative learning platform, which, in turn, helps in both teaching and learning abstract concepts in medicine, which requires of visual and manipulable objects difficult to obtain, due to the large space they occupy in magnetic media or because of how difficult it is to get their models in physical form. The proposed system strengthens the anatomical identification process in the area of medicine, specifically in the physiological activity of the human heart. In addition, this system allows interaction with the students, through which certain body parts of the human heart are identified, and, consequently, facilitates their learning with an iterative operation. Finally, the system is focused, so that the student uses his/her sense of sight, hearing, and kinesthetic, which, together, will allow a better assimilation of knowledge.",signatures:"Gerardo Reyes-Ruiz and Marisol Hernández-Hernández",downloadPdfUrl:"/chapter/pdf-download/70925",previewPdfUrl:"/chapter/pdf-preview/70925",authors:[{id:"313803",title:"Dr.",name:"Gerardo",surname:"Reyes",slug:"gerardo-reyes",fullName:"Gerardo Reyes"},{id:"313837",title:"Prof.",name:"Marisol",surname:"Hernández Hernández",slug:"marisol-hernandez-hernandez",fullName:"Marisol Hernández Hernández"}],corrections:null},{id:"71251",title:"An Interactive VR System for Anatomy Training",doi:"10.5772/intechopen.91358",slug:"an-interactive-vr-system-for-anatomy-training",totalDownloads:773,totalCrossrefCites:3,totalDimensionsCites:5,hasAltmetrics:1,abstract:"In recent decades, virtual reality (VR) becomes a potential solution to enhance clinical medical (functional reeducation, training, etc.), especially with the growth evolution of technologies form both visualization (e.g., HoloLens, VR in Case, etc.) and 3D gestural interaction (Ray Casting, Free Hand, etc.) point of views. The 3D visualization of the human anatomy could be a serious asset for students in medicine. This new technology could provide a clear and realistic representation of the internal organs of the human body, without having to resort to surgery. 3D organs based-course supports visualization could be a useful tool for students, especially in their first graduate studies, to enhance their perception on human’s internal composition. This system is composed of two modules, 3D human’s anatomy visualization module and interaction module for organs manipulation. Finally, the system will be tested and evaluated with several subjects.",signatures:"Djamel Aouam, Nadia Zenati-Henda, Samir Benbelkacem and Chafiaa Hamitouche",downloadPdfUrl:"/chapter/pdf-download/71251",previewPdfUrl:"/chapter/pdf-preview/71251",authors:[{id:"64814",title:"Mr.",name:"Samir",surname:"Benbelkacem",slug:"samir-benbelkacem",fullName:"Samir Benbelkacem"},{id:"72390",title:"Dr.",name:"Nadia",surname:"Zenati-Henda",slug:"nadia-zenati-henda",fullName:"Nadia Zenati-Henda"},{id:"314338",title:"Ph.D. Student",name:"Djamel",surname:"Aouam",slug:"djamel-aouam",fullName:"Djamel Aouam"},{id:"318975",title:"Dr.",name:"Chafiaa",surname:"Hamitouche",slug:"chafiaa-hamitouche",fullName:"Chafiaa Hamitouche"}],corrections:null},{id:"71106",title:"Learning by Augmented Reality: Cluster Analysis Approach",doi:"10.5772/intechopen.91252",slug:"learning-by-augmented-reality-cluster-analysis-approach",totalDownloads:624,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:0,abstract:"Because the use of augmented reality (AR) is increasing, it is important to study its possibilities within both formal and informal learning contexts. We clustered 146 sixth graders using AR at a science center based on their reasoning, motivation, and science learning results using the self-organizing maps method (SOM) to identify AR-using subgroups. The aim was to consider reasons why the AR method could be of more beneficial for some students than others. The clustering results complemented earlier findings on AR gains in learning, as an unexpected response to intervention was discovered using this nonlinear analysis. The previous results had indicated that after the AR experience, science test results generally improved and particularly among students with the lowest achievement. The SOM-clustering results showed a majority group of boys, especially those interested in science learning both at school and at the science center using AR. Despite low school achievement, their high motivation led to good science learning results. The prior results, according to which girls closed the science knowledge gap between boys after using AR, became more relative, as two girl-dominated subgroups were identified. The reasons for the results were considered on the basis of motivation, multimedia learning theory, and concept formation theories.",signatures:"Helena Thuneberg and Hannu S. Salmi",downloadPdfUrl:"/chapter/pdf-download/71106",previewPdfUrl:"/chapter/pdf-preview/71106",authors:[{id:"314465",title:"Prof.",name:"Hannu",surname:"Salmi",slug:"hannu-salmi",fullName:"Hannu Salmi"},{id:"314498",title:"Dr.",name:"Helena",surname:"Thuneberg",slug:"helena-thuneberg",fullName:"Helena Thuneberg"}],corrections:null},{id:"71263",title:"3D Modeling and Computer Graphics in Virtual Reality",doi:"10.5772/intechopen.91443",slug:"3d-modeling-and-computer-graphics-in-virtual-reality",totalDownloads:1038,totalCrossrefCites:5,totalDimensionsCites:5,hasAltmetrics:1,abstract:"In the era of digital information technologies, 3D modeling and computer graphics techniques not only apply to the development of virtual models for computer simulation, artificial intelligence (AI), big data analytics, etc., but also they can be applied in many different applications in virtual reality (VR). However, the computer graphics effect and visual realism are usually the trade-offs with the real-time and realistic interaction in VR. In this book chapter, we would like to review the general flow of the VR program development process, and the recent 3D modeling and texture painting techniques used in VR. On the other hand, we would introduce some of the key 3D modeling and computer graphics techniques that can be applied in VR in order to enhance the speed of interaction. The key techniques including smoothing techniques and mesh editing modifiers are not only useful for the designers to learn the 3D modeling process, but it also helps to create less complex mesh models maintaining good visual effects. The techniques are particularly important in the development of 3D models to satisfy the demanding computation requirement of real-time interaction in VR program.",signatures:"Yuk Ming Tang and H.L. Ho",downloadPdfUrl:"/chapter/pdf-download/71263",previewPdfUrl:"/chapter/pdf-preview/71263",authors:[{id:"314714",title:"Dr.",name:"Yuk",surname:"Tang",slug:"yuk-tang",fullName:"Yuk Tang"}],corrections:null},{id:"72385",title:"3D Solid Reconstruction from 2D Orthographic Views",doi:"10.5772/intechopen.91977",slug:"3d-solid-reconstruction-from-2d-orthographic-views",totalDownloads:672,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:0,abstract:"Three-dimensional computer-aided design (CAD) models are widely used by designers because of their useful applications in the areas of CAD/CAM/CAE/CAQ. A desirous trend to create this model, which has long been studied by scientists around the world, is a 3D model reconstruction from 2D orthographic views. With this method, it is easy to enter geometric information as well as use 2D drawings that have already existed. Most of the previous works used three views, but many of the mechanical parts needed only two views. An advanced 3D solid reconstruction system using only two orthographic views is the subject of this chapter. The proposed method has been implemented and verified reliability by an ObjectARX program plugged into AutoCAD 2018. The 3D models have been checked for their compatibility with 3D CAD/CAM systems. This chapter presents principles, algorithms, databases, programming for the advanced reconstruction system, and some of its technical applications.",signatures:"Long Hoang",downloadPdfUrl:"/chapter/pdf-download/72385",previewPdfUrl:"/chapter/pdf-preview/72385",authors:[{id:"310032",title:"Ph.D.",name:"Long",surname:"Hoang",slug:"long-hoang",fullName:"Long Hoang"}],corrections:null},{id:"73091",title:"Blockchain-Based Data Integrity for Collaborative CAD",doi:"10.5772/intechopen.93539",slug:"blockchain-based-data-integrity-for-collaborative-cad",totalDownloads:855,totalCrossrefCites:0,totalDimensionsCites:2,hasAltmetrics:1,abstract:"Distributed and collaborative computer-aided design (CAD) environments include building information modeling (BIM) and geographical information systems (GISs) in civil engineering and architecture, or product data management/product life cycle management (PDM/PLM) in mechanical engineering. It is essential to keep the data integrity in these computer applications as it contributes to buildingusers’ confidence in CAD/BIM/PDM data. Blockchain technology, the core foundation of cryptocurrencies, is increasingly being used for other purposes and could solve the data integrity issue in collaborative CAD environments. However, it has some disadvantages such as the transparency of data and the slowness of storing data in the blockchain due to distributed consensus. Increasing demand by the Industry 4.0, IoT, Smart Cities, and other initiatives could foster the best what blockchain has to offer: data integrity, reliability, and traceability. This chapter explains how blockchain works, how can it be utilized in distributed CAD environments, what are the major challenges for implementation, and how CAD vendors could use it to increase CAD data integrity.",signatures:"Samir Lemeš",downloadPdfUrl:"/chapter/pdf-download/73091",previewPdfUrl:"/chapter/pdf-preview/73091",authors:[{id:"167012",title:"D.Sc.",name:"Samir",surname:"Lemes",slug:"samir-lemes",fullName:"Samir Lemes"}],corrections:null},{id:"72350",title:"Mixed Reality in the Presentation of Industrial Heritage Development",doi:"10.5772/intechopen.92645",slug:"mixed-reality-in-the-presentation-of-industrial-heritage-development",totalDownloads:632,totalCrossrefCites:0,totalDimensionsCites:1,hasAltmetrics:0,abstract:"The chapter ‘Mixed reality in the presentation of industrial heritage development’ is aimed at exploring opportunities for collaboration between theoretical research, monument preservation, virtual reality and architectural practice. It deals with the identified key factors that conditionally affect the quality and efficiency of architectural design process of architects within the cooperation in the conservation process of industrial heritage as well as the opportunities of transfer the research results from futuristic disciplines. For this purpose, the chapter examines the case study ‘the reconstruction of Old Power Plant in city Piešťany’ and describes possible solutions on the basis of the Mixed reality (MR). The opportunity to experience the industrial object with multiple senses (sight, hearing, smell, touch) in MR delivered a unique personalized experience and immersive memories about lost heritage.",signatures:"Vladimír Hain and Roman Hajtmanek",downloadPdfUrl:"/chapter/pdf-download/72350",previewPdfUrl:"/chapter/pdf-preview/72350",authors:[{id:"312940",title:"Ph.D.",name:"Vladimír",surname:"Hain",slug:"vladimir-hain",fullName:"Vladimír Hain"},{id:"312942",title:"Dr.",name:"Roman",surname:"Hajtmanek",slug:"roman-hajtmanek",fullName:"Roman Hajtmanek"}],corrections:null},{id:"72291",title:"Stereoscopy and Autostereoscopy",doi:"10.5772/intechopen.92633",slug:"stereoscopy-and-autostereoscopy",totalDownloads:535,totalCrossrefCites:1,totalDimensionsCites:1,hasAltmetrics:0,abstract:"For a seamless Mixed Reality visual experience the display device needs to be versatile enough to enable both 2D as well as 3D Stereoscopic and Autostereoscopic see through information display. The ability to enable single viewer 3D stereoscopic information display is now relatively mature and easier to accomplish but is still a challenge for multiple concurrent users. In addition, the ability to enable virtual reality information display for single viewer is now also relatively mature. However, the ability to enable seamless augmented reality information onto a 3D world is relatively more challenging. It is orders of magnitude, more challenging to have a mixed reality display approach that includes all these capabilities. This chapter will provide a treatise on the stringent requirements for autostereoscopic information display as well as switchable 2D-3D autostereoscopic information displays as a guide for designing better mixed reality displays. It will then conclude by providing an alternative approach for a switchable 2D-3D see through Mixed Reality information display.",signatures:"Wallen Mphepo",downloadPdfUrl:"/chapter/pdf-download/72291",previewPdfUrl:"/chapter/pdf-preview/72291",authors:[{id:"319846",title:"Dr.",name:"Wallen",surname:"Mphepo",slug:"wallen-mphepo",fullName:"Wallen Mphepo"}],corrections:null},{id:"72705",title:"Mixed Reality: A Known Unknown",doi:"10.5772/intechopen.92827",slug:"mixed-reality-a-known-unknown",totalDownloads:953,totalCrossrefCites:1,totalDimensionsCites:3,hasAltmetrics:0,abstract:"Mixed reality (MR) is an area of computer research dealing with the combination of real-world and computer-generated data (virtual reality), where computer-generated graphical objects are visually mixed into the real environment and vice versa in real time. This chapter contains an introduction to this modern technology. Mixed reality combines real and virtual and is interactive, real-time processed, and registered in three dimensions. We can create mixed reality by using at least one of the following technologies: augmented reality and augmented virtuality. The mixed reality system can be considered as the ultimate immersive system. MR systems are usually constructed as optical see-through systems (usually by using transparent displays) or video see-through. Implementation of MR systems is as marker systems (real scene will be added with special markers. These will be recognized during runtime and replaced with virtual objects) or (semi) markerless systems (processing and inserting of virtual objects is without exact markers. Additional information is usually needed, for example, image and face recognition, GPS coordinates, etc.). 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The number of flights has increased by 80% between 1990 and 2014 and is forecasted to grow by a further 45% between 2014 and 2035. Consequently, the future growth in the European aviation sector will be inextricably linked to its environmental sustainability [1].
\nDuring the last decade, a lot of studies have also focused on the aircraft emissions impact on local and regional air quality in the vicinity of airport [2, 3, 4, 5, 6, 7]. The basic objects of attention are extremely high concentration of toxic compounds (including nitrogen oxides (NOx), particle matter (PM with various sizes: PM10, PM2.5, and ultrafine), unburned hydrocarbons (UHC), and carbon monoxide (CO)) due to airport-related emissions and their significant impact on the environment [2, 8] and health of the people living near the airport [3, 4].
\nGround-level emissions associated with the airport have the biggest impact on local air quality, whereas elevated aircraft emissions have less impact because they take place at increasing height. Figure 1 shows aircraft produce approximately 54% of ground-level emissions, whereas airport-related traffic is estimated to emit a further 28% [5].
\nEstimated ground-level airport-related emissions from Heathrow Airport.
Analysis of inventory emission results at major European (Frankfurt am Main, Heathrow, Zurich, etc.) and Ukrainian airports highlighted that aircrafts (during approach, landing, taxi, takeoff and initial climb of the aircraft, engine run-ups, etc.) are the dominant source of air pollution in most cases under consideration [6, 9, 10], Figures 2 and 3. More than 50% of total NOx emissions inventory inside airport area is released by aircraft engines. As shown in Figures 2(b) and 3(b), the contribution of aircraft emission to total airport PM emissions is sufficiently high.
\nThe emissions inventory of NOx [(a) annual emissions: 3.284 tons/year] and PM10 [(b) total emissions: 25 tons/year] within the Frankfurt International Airport for 2005 with an intensity of takeoffs and landings, 1300 per day.
The emissions inventory of NOx (a) and PM10 (b) within Boryspil International Airport with an intensity oftakeoffs and landings 50,000 per year.
Considered problems are intensified in connection with rising tensions of expansion of airports and growing cities closer and closer each other (the most urgent is for Ukrainian airports, such as Zhulyany, Boryspil, Lviv, Odessa, and Zaporizhzhia) and accordingly growing public concern with air quality around the airport.
\nAircrafts are a special source of air pollution due to some features.
\nJet structure for jet transport model. ΔhA, XA are the height and longitudinal coordinate of jet axis rise due to buoyancy effect, m; hEN is the height of engine installation, m; RB is the radius of jet expansion, m; X1 is the longitudinal coordinate of first contact point of jet with ground, m; and X2 is the longitudinal coordinate of a point of jet lift-off from the ground due to buoyancy effect, m.
So, to evaluate the aircraft contribution in Local Air Quality assessment of the airports accurately, it is important to take in mind few features of the aircraft during their landing-takeoff cycle (LTO), which define emission and dispersion parameters of the considered source.
\nModeling of airport air pollution includes two parts: emission inventory and dispersion calculation.
\nICAO Doc 9889 [12] recommends few tools for air quality analysis—to model emission inventory from every character groups of the spatially distributed sources as well as atmospheric concentrations resulting from emission dispersion: EDMS is based on Gaussian plume model (AERMOD) [13], LASPORT is based on Lagrangian particle model (LASAT) [14], and ALAQS–AV provides to use both Gaussian and Lagrangian approaches for dispersion calculations [12].
\nA complex model Pollution and Emission Calculation (PolEmiCa) for assessment of air pollution and emission inventory analysis, produced within the airport boundaries, has been developed at National Aviation University (Kyiv, Ukraine) [15]. It consists of the following basic components:
The emission inventory of aircraft emissions are usually calculated on the basis of certificated emission indexes, which are provided by the engine manufacturers and reported in the database of the International Civil Aviation Organization (ICAO) [16].
\nThe emission indices rely on well-defined measurement procedure and conditions during aircraft engine certification. Under real circumstances, however, these conditions may vary and deviations from the certificated emission indices may occur due to the impact factors such as
the life expectancy (age) of an aircraft—emission of an aircraft engine might vary significantly over the years (the average period is 30 years); usually aging aircraft/engine provides higher emission indices in comparison with same type but new ones;
the type of an engine (or its specific modification, for example with different combustion chambers) installed on an aircraft, which can be different from an engine operated in an engine test bed (during certification); and
meteorological conditions—temperature, humidity, and pressure of ambient air, which can be different for certification conditions.
So, the analysis of several measurement campaigns for idling aircraft at different European airports (London-Heathrow in 1999 and 2000, Frankfurt/Main in 2000, Vienna in 2001, and Zurich in 2003) [7] concludes that the largest difference between emission indices’ measurement data and the ICAO data for CO for the RB211-524D4 engine was caused due to quite long life expectancy of B747-236 (aging aircraft and engines) (Figure 5). The oldest aircraft with an emission index of 52.9 g/kg was 25 years old; the other two were built in 1987 and 1983. Mean values of the measured emission indices for three engine types (CFM56-5B1, CFM-5B4/2P, and CFM56-5B3/P) are nearly identical although the ICAO data of the CFM56-5B family differ by a factor of 2 (Figure 6
Comparison measured EICO by FTIR emission and absorption spectrometry during measurement campaign for idling aircraft at the European airports.
Comparison EICO determined for CFM-5Bx engines with ICAO values for idling aircraft at European airports.
The dependences of engine thermodynamic parameters and EE index for NOx (assessed in g/kgfuel) and factor Q (assessed in g/sec) for the aircraft engine D-36 (installed on Yakovlev-42 and on Antonov-74, -148, and -158 aircrafts) are shown in Figure 7 as the functions from ambient temperature ТА (basic engine control law for D-36 provides the constant value of compressor pressure ratio π∑* in a broad range of ambient temperatures). Values of an emission index ЕINOx vary up to 50% in relation to value at International standard atmosphere conditions inside the range of ambient temperatures between −30 and + 30°C [17, 18].
\nDependences of EE index EI [gemission/kgfuel], factor Q [g/s] for NOx, and temperature behind the compressor Tc for D-36 engine from ambient temperature.
A gradient of change of the factor
So, under operating conditions, engine emission characteristics are subject to changes as a result of influence of the meteorological factors.
\nBased on the obtained research outcomes of aircraft engine emission derivation, due to meteorological factor influences, the model was developed to recalculate the emission indices for ISA conditions
For emission factor (in g/s or kg/hour), the recalculation into actual meteorological conditions are determined under the formula:
\nIn Table 1, the correction coefficients for NOx emission factor KQnox and for products of incomplete fuel combustion KQco for average parameters of the engines while in operation are adduced.
\nTemperature, °C | \n−20 | \n−10 | \n0 | \n+ 10 | \n+ 20 | \n
---|---|---|---|---|---|
Factor KQnox\n | \n0,74 | \n0,81 | \n0,88 | \n0,96 | \n1,0 | \n
Factor KQco\n | \n1,3 | \n1,2 | \n1,1 | \n1,04 | \n1,0 | \n
Average values of aircraft engine emission factor recalculation into actual ambient temperature.
Current calculation method, realized in software PolEmiCa, also implemented the recommendations of ICAO Doc9889 [12] for emission factor assessment, including the recommendations for aircraft engine emission.
\nThe efficiency of the temperature (seasonal) factor account for pollution inventory produced by aircraft in airport area is shown in Table 2 by matching the outcomes of calculation from previous and new calculation techniques [19].
\nTechniques | \nCO | \nHC | \nNOx\n | \nPM | \n
---|---|---|---|---|
Previous | \n307,000.1 | \n104,200. | \n16,700.0 | \n3400.0 | \n
ICAO LTO | \n282,754.6 | \n97,139.2 | \n18,621.1 | \n2859.4 | \n
Actual LTO for considered airport | \n185,055.1 | \n59,556.4 | \n16,869.1 | \n2207.3 | \n
Actual LTO for considered airport + temperature factor | \n190,246.1 | \n61,254.1 | \n15,984.1 | \n2207.3 | \n
Calculated aircraft engine pollution, kg.
There are different types of engines installed on civilian aircraft currently: turbojet (TJE), turbofan (TFE), turboprop (TPE), and piston (PE). The process of contaminant transport by engine jet is described by the theory of turbulent jets [20]. The restrictions on the use of this theory are satisfied completely in the current task [21]: efflux from a jet engine is a very complex fast flow of hot gas, it is nonuniform, turbulent, and has various velocity scales and chemical reactions; the gas flow in jet is usually isobaric process, the pressure in the jet flow is equal to the atmospheric pressure, which is corresponding to the nature of incompressible flow; the Mach number of jet flow at outlet nozzle of the engine does not exceed 1; and the Reynolds number for the flow is rather large U0D0/ν > 105, and the initial turbulence in the jet flow is quite moderate. For majority of the calculations, the simplifying preconditions were formulated and used: radial velocity profile has a self-preserving pattern; mechanisms of boundary layer formation near ground surface are not taken into account in this calculation; the external borders of a jet represent linear dependencies; the structure of shear layer is similar to free jet [11].
\nThe conditions of jet outflow define the type of its physical model and appropriate algorithm of its parameters calculation. The choice of the model depends on the direction of the jet at exhaust nozzle relative to the direction of the wind and/or airplane motion and from the speeds of the jet, airplane, and wind. The initial parameters for jet calculations are: slipstream flow parameter m = UH/U0, where U0 is the velocity of the jet at engine nozzle, m·s−1 and UH is the speed of an external air flow, m·s−1; UH = UW + UPL, where UW is the wind speed, m·s−1 and UPL is the airplane speed, m·s−1; Nen – number of the engines in operation, angle between vectors of wind and jet speeds ψ, grad. For ground stages of LTO cycle in airport area, the slipstream parameter m < < 1; therefore, in most cases, it is possible to take advantage of semiempirical modeling of the nonisothermal-free jets.
\nTurbulent-free jet can be divided into three stages: initial (potential core), transitive (flow development region), and developed (fully developed flow) [20]. Their boundaries along the length of jet axis
\n
\n
where \n
The stage of a jet, which is defined by boundary
At point (
where
For an estimation of the buoyancy characteristics, the Archimedes number is introduced:
\nThe height of the jet is given by the empirical relationship [23]:
\nwhere \n
The concentration is changed along the length of jet in dependence with its type. Taking into account that flow parameter
where C0 is the concentration at the exhaust nozzle of the engine, μg·m−3; KC = 9.5 for the free jet, KC = 6.5—for an opposite jet; and KE takes into account influence of a reflecting surface on straightline characteristics of a jet: ĥEN < 20 KE = 1–0.025hEN, at ĥEN ≥ 20, KE = 1, where ĥ = h/R0.
\nConsidered version of complex model PolEmiCa is based on a semiempirical model of turbulent jets and not taking into account ground surface impact on jet structure and its behavior [11]. It was argued that development of three-dimensional model of exhaust gases jet from aircraft engine near the ground is an important research topic for airport LAQ [24, 25, 26].
\nA three-dimensional model of a jet was generated in Fluent 6.3 by using large Eddy simulation (LES) method to reveal the unsteady ground vortices and turbulence characteristics of fluid flow, to investigate transient parameters of hot gases in jet and their dispersion.
\nThe jet from aircraft engine exhaust near ground surface is corresponding to a wall jet if an aircraft is moving on this surface. Numerical simulation of wall jets was performed in Fluent 6.3 for engine NK-8-2 U of the aircraft Tupolev-154 for different operational conditions.
\nFor the considered task, a computational domain was built to simplify the problem and optimize the mesh distribution where it is needed mostly (i.e., near the engine exhaust and ground surface) (Figure 8).
\nGeometry model and computational mesh visualization in vertical plane.
The zone of ground vortices formation—between ground surface and aircraft engine exhaust nozzle—is characterized by structured mesh with higher resolution, with an aim to investigate the ground vortices generation processes and basic mechanisms of boundary layer formation, ground surface impact on fluid flow mechanics, and particularly Coanda effect occurrence. Zone of engine nozzle exhaust is discretized using a very fine structured mesh to capture the jet development pattern and its vortices structure [24, 25].
\nFor considered task, the boundary conditions were specified to the boundaries of the computational domain of jet flow field (Figure 9).
\nBoundary conditions for CFD simulations of exhaust gases of jet from aircraft engine near ground.
LES provides an approach inside which large eddies are explicitly resolved in time-dependent simulation using low-pass-filtered Navier-Stokes equations [25]. Smagorinsky’s subgrid model was set to model the smaller eddies (fluctuation component of instantaneous velocity of modeling fluid flow) that are not resolved in the LES. All the calculations were made with a second-order discretization.
\nComparison of results from numerical simulations of free and wall jets for engine idle operation (U0 = 50 m·s−1; T0 = 343 K) revealed some differences in their structures and properties.
\nAxial velocity profiles based on Fluent 6.3 results show (Figure 10) a substantial difference between the wall and free jet. First, the decay rate is 40–50% higher for free jet than for the wall jet. In the case of wall jet, the maximum velocity is high and equal to 50% of initial velocity at a distance of 90 diameters of the jet penetration, whereas the free jet is relatively slow and equal only to 10% of the velocity at exhaust nozzle of the engine, Figure 10. Second, the wall jet penetrates deeper (SBwall ≈ 150 m) than the free jet (SBfree ≈ 100 m) (Figure 11). As shown in Figure 12, jet arises over the ground surface due to buoyancy effect much faster (longitudinal coordinate, XA = 65 m) and higher for free jet (height of plume rise, ΔhA = 17.8 m), than in case of wall jet (XA = 135 m, ΔhA = 14 m).
\nMaximum velocity decay along the axis of the free and wall jets.
Mean velocity contours for (a) free jet and (b) wall jet in streamwise direction after 10 s.
Buoyancy effect of free and wall jets: longitudinal and vertical coordinates of jet axis.
The same differences in the structure and properties of free and wall jets were revealed for different operational conditions (U0 = 100 m·s−1; T0 = 343 ÷ 673 K).
\nThe ground surface sufficiently impacts on jet’s structure and behavior. Numerical simulations of wall jet by Fluent 6.3 defined a decrease of buoyancy effect of height rise, which is 3–5 times less (Figure 13a) and an increase of longitudinal coordinate of jet penetration by 30%, (Figure 13b).
\nComparison of buoyancy effect parameters calculated by Fluent 6.3 and complex model PolEmiCa: longitudinal coordinate (a) and height of jet rise (b).
Comparison of the calculated parameters of the jet (height and longitudinal coordinate of jet axis arise due to buoyancy effect, length of the jet penetration) by Fluent 6.3 and semiempirical model for aircraft engine jets implemented in complex model PolEmiCa proves the found trend of the jet behavior. Thus, the including the ground impact on the jet structure and its behavior by Fluent 6.3, provides longitudinal coordinate increase and height reduction of buoyancy effect.
\nThe basic model equation for definition of instantaneous concentration
where
where
According to considered formula (11), a dispersion model integrates engine emission model and jet transport model via including the following parameters:
\n\n
\n
In other words, engine emission model and jet transport model provide input data to calculate concentration values by the dispersion model.
\nThe development of three-dimensional model of wall jet by using CFD tool (Fluent 6.3) allows to include the ground impact on basic parameters of the exhaust gases jet (i.e., plume buoyancy effect, length, and dispersion characteristics) for further dispersion modeling (11). It may be concluded that using the CFD tool allows us to improve the PolEmiCa model by taking into account the impact of ground surface on the jet structure and its behavior. So, it means that the improvement is achieved with input parameters for further dispersion calculation.
\nThe verification of the PolEmiCa model with measurement data was done initiatively for trials made in airports of Athens (Greece, 2007) [27] and Boryspil (Ukraine, 2012) [28]. In both cases, the comparisons were quite good, showing appropriate correspondence of the model to subject of assessment.
\nComparison between calculated and measured NOx concentrations (averaged for 1 min) in aircraft engine plume under real operation conditions (aircraft accelerating on the runway during takeoff stage of flight) at Athens airport is shown in Table 3 and Figure 14.
\n№ | \nAircraft | \nEngine | \nCalculated concentration | \nMeasured concentration | \n||
---|---|---|---|---|---|---|
NOx (delta), μg/m3\n | \nNOx (delta), μg/m3\n | \n|||||
With jet | \nWithout jet | \nValue | \nError | \n|||
1 | \nB737-3YO | \nCFM56-3C1 | \n27,43 | \n30,01 | \n31,8 | \n3,2 | \n
2 | \nB737-3Q8 | \nCFM56-3B2 | \n30,7 | \n33,50 | \n28,0 | \n2,8 | \n
3 | \nВ737-45S | \nCFM56-3B2 | \n29,76 | \n27,95 | \n23,6 | \n2,4 | \n
4 | \nB737-4Q8 | \nCFM56-3B2 | \n31,28 | \n34,93 | \n56,9 | \n5,7 | \n
5 | \nA-310 | \nCF6-80C2A8 | \n88,86 | \n122,12 | \n86,1 | \n8,6 | \n
6 | \nA-319 | \nCFM56-5B5 | \n29,85 | \n32,27 | \n26,9 | \n2,7 | \n
7 | \nB747–230 | \nCF6-50E2 | \n163,63 | \n205,37 | \n82,5 | \n8,2 | \n
8 | \nA-321-211 | \nCFM56-5B-3 | \n81,78 | \n89,74 | \n43,3 | \n4,3 | \n
9 | \nA320–214 | \nCFM56-5B-4 | \n49,99 | \n52,29 | \n16,4 | \n1,6 | \n
10 | \nB737-33A | \nCFM56-3B1 | \n25,5 | \n27,95 | \n11,5 | \n1,1 | \n
Measurement results by TE42C-TL96 system and calculation results by PolEmiCa model of NOx concentration in plume from aircraft engine emission for maximum operation mode.
Comparison of measured and modeled averaged concentrations of NOx (for a period of 1 min) under takeoff conditions (maximum operation mode of aircraft engine).
Besides, results were defined for the cases with and without jets from the engines to show that with jets, they are more equal (by 17%) to measured data, because impact of jet basic parameters (buoyancy effect and dispersion characteristics) on concentration distribution was estimated by complex model PolEmiCa (Table 3 and Figure 14). Comparison between measurements and the PolEmiCa/Fluent 6.3 model is significantly better (by 20%), because lateral wind and ground impact on jet parameters (height of buoyancy effect, jet length penetration, and plume dispersions) were included in the model.
\nThe better agreement was obtained between the calculated and measured instantaneous concentration (averaged for 3 s) in aircraft engine jet under real operation conditions (aircraft accelerating on the runway and takeoff) at Boryspil airport.
\nAs shown from Table 4 and Figure 15, the modeling results for each engine are in good agreement with the results of measurements by the AC3 2 M system due to taking into account the jet- and plume regime during experimental investigation at Boryspil airport. Also, using CFD code (Fluent 6.3) allows to improve results by 30% (coefficient of correlation, r = 0.76) by taking into account lateral wind and ground impact on jet parameters.
\nAircraft | \nAircraft engine | \nELAN | \nAC3 2 M | \nPolEmiCa CFD (Fluent 6.3) | \nPolEmiCa | \n|||||
---|---|---|---|---|---|---|---|---|---|---|
Peak 1 | \nPeak 1 | \nBackground | \n3 м | \n6 м | \n1 engine | \nAll engines | \n1 engine | \nAll engines | \n||
NOx | \nNOx | \nNOx | \nNOx | \nNOx | \nNOx | \nNOx | \nNOx | \nNOx | \n||
BAE147 | \nLY LF507-1H | \n38 | \n35 | \n1,70 | \n22,067 | \n33,9 | \n35,1 | \n70,46 | \n48,9 | \n202,3 | \n
A321 | \nCFM56-5B3/P | \n39 | \n39 | \n0,72 | \n44,00 | \n54,2 | \n90,85 | \n182,90 | \n184,2 | \n371,2 | \n
B735 | \nCFM-563C1 | \n40 | \n45 | \n0,77 | \n94,095 | \n76,57 | \n60,03 | \n120,91 | \n35,3 | \n71,10 | \n
B735 | \nCFM56-3B1 | \n45 | \n41 | \n1,74 | \n29,20 | \n23,4 | \n42,34 | \n85,30 | \n33,7 | \n67,76 | \n
Comparison measured (AC3 2 M, ELAN) and calculated concentration (averaged for 3 s) of NOx produced by aircraft engine emissions at accelerating stage on the runway.
Comparison of the PolEmiCa and PolEmiCa/CFD model results with the measured NOx concentration at different heights for selected aircraft engines under maximum operation mode.
Analysis of inventory emission results at the major European and Ukrainian airports highlighted that aircrafts (during approach, landing, taxi, takeoff and initial climb of the aircraft, engine run-ups, etc.) are the dominant source of air pollution in most cases under consideration. The aircraft is a special source of air pollution. Thus, the method for LAQ assessment of the airports has to take in mind few features of the aircraft during their landing-takeoff cycle (LTO), which defines emission and dispersion parameters of the considered source.
\nCFD numerical simulations of aircraft engine exhaust jet near to ground surface show that structures, properties, and fluid mechanics of jets are influenced by the ground surfaces, providing longer penetration, less rise, and appropriate dispersion parameters of the jets, and accordingly little bit higher concentrations of air pollution. So, using results obtained from CFD simulations (Fluent 6.3) of aircraft engine jet dynamics allow us to improve LAQ modeling systems (improved version of PolEmiCa).
\nComparison of measured and modeled NOx concentrations in the plumes from aircraft engines was significantly improved (by 20%—at Athens and by 30%—at Boryspil airports) by taking into account lateral wind and ground impact on jet parameters (height of buoyancy effect, jet length penetration, and plume dispersions).
\nThe word epigenetics comes from the Greek word ‘epi’ that means above; that is, hereditary variations in phenotype that do exclude alterations in the nucleotide sequence in DNA [1]. Epigenetic mechanisms involve DNA methylation, post-translational histone modifications, and noncoding RNAs (ncRNAs) [1]. Many studies focus on the epigenetic mechanisms of various diseases. Epigenetic processes are essential for the healthy growth and development of an organism [1]. Epigenetic mechanisms are implicated in the expression of circadian genes in the suprachiasmatic nucleus (SCN) neurons and peripheral tissues [2]. The accumulation of lifestyle and age-related epigenetic changes could result in the development of metabolic disorders and atherosclerosis [2].
The influence of epigenetic changes on the cardiovascular system is an essential link between genotype to phenotype diversity [3]. Epigenetic changes are potentially reversible and may be affected by environmental factors, nutrition, as well as gene-environment interactions. Identifying and understanding epigenetic factors represent a new insight into our knowledge of the risks of cardiovascular disease (CVD) [1].
The circadian clock is a preserved system that allows organisms to adapt to frequent daily variations, such as the day and night and food availability [4]. This center clock receives signals from the environment and coordinates the daily activity of peripheral clocks found in almost all tissues [4]. The molecular clock is vital in maintaining metabolic and physiological homeostasis [5]. The circadian clock is linked to cellular metabolism so that dysregulation of the circadian rhythm can contribute to various pathological conditions such as diabetes, obesity, metabolic syndrome, inflammation, sleep disorders, and CVDs [5, 6, 7, 8].
Genome-wide studies show that 10–15% of all transcripts have a circadian pattern in different tissues involved in the control of metabolism, such as the cardiovascular function [4, 6, 8, 9]. The onset of ischemic cardiopathy is irregularly distributed during the day [1, 10, 11]. A chronobiological strategy to heart disease may present new possibilities to enhance drug development to improve therapeutic outcomes [1]. Genetic evidence supports the function of circadian rhythm in the adjustment of metabolism.
Cardiovascular diseases are complex and diverse. They include hypertension, coronary artery disease, heart failure, and stroke and are a main worldwide reason for morbidity and death in advanced economies and carry a substantial economic burden [1, 3, 12, 13, 14, 15]. CVDs are associated with a variety of hereditary and variable risk factors, but environmental and genetic impacts may explain a smaller fraction of CVD risk variability [1, 12]. Studies showed that there is a wide range between 40 and 80% of the genetic contribution to the onset of cardiovascular disease [16].
The complex pathogenesis of CVD is due to the abundance of genetic and environmental factors, of which epigenetic changes are a significant factor [3]. Several risk factors of CVD, like diet, smoking, stress, circadian rhythm, and pollution, are related to epigenetic modifications [1]. Disorders such as hypertension, diabetes, and obesity are often utilized to recognize and cure people at increased CVDs risk [1]. Epigenetic modifications are associated with the processes involved in the CVD in humans or directly affect the gene expression involved in a major cardiac complication, myocardial infarction (MI). Hypertension is one of the leading causes of CVDs [3], while insulin resistance is one of the most significant precursors of type 2 diabetes and associated cardiometabolic conditions [17].
Changes in the style of living and diet could decrease the risk of CVDs [14]. Epigenetic factors indicate there is interindividual variability from birth. It can be stable over the life span and is considered to be an initiator of early programming for adult-onset diseases [12, 18]. The understanding of epigenetics in the onset of CVDs may provide a new perspective on diseases [14].
Epigenetics studies heritable variations in gene expression that exclude any change in the DNA sequence [16, 19]. Epigenetic changes include modifications of the DNA base, post-translational histone modifications, and ncRNA mechanisms that run in the nucleus [16, 20]. The epigenome moves the genome from a transcriptionally active to a transcriptionally inactive state [4, 21]. Epimutation transmissions occur throughout the life of the individual [2]. The rate of epigenetic variation is higher than that of genetic mutations because the formation of new inherited changes allows adjustment to a new environment [14, 16].
The most studied epigenetic change is cytosine methylation. It is also a method for suppressing gene expression [22]. DNA methyltransferase (DNMT) enzymes perform DNA methylation. DNMTs bind the methyl group to the 5-site cytosine [16]. The methyl group most commonly binds to the cytosine at a CpG site. It is the fundamental and ubiquitous epigenetic mechanism [14]. The DNMT enzyme family, consisting of DNMT1, DNMT3a, and DNMT3b, methylates cytosine into 5-methylcytosine [14]. Promoter methylation is usually connected with inhibition of transcription [14]. DNMT1 controls the mitotic inheritance of methylated DNA, while DNMT3a and DNMT3b are mainly in charge of
Nucleosomes are composed of histone proteins around which DNA is wound into chromatin [16]. Nucleosomes consist of eight histone proteins: two dimers of H2A/H2B and two dimers of H3/H4. Each histone has an adjustable amino-acid tail [16]. Histones can change at more than 30 amino acid residues within amino-terminal tails [4]. Histone modifications include various processes such as acetylation, methylation, phosphorylation, sumoylation, and ubiquitination. It has a function in the organization of chromatin composition and gene expression by altering the intensity of chromatin condensation [1, 14, 23]. Histones are mostly acetylated on lysine (K) residues. Histone acetyltransferase (HAT) and histone deacetylase (HDAC) regulate histone acetylation [14]. Histone methyltransferase regulates histone methylation, while histone demethylase catalyzes demethylation. Transcription activation is usually associated with acetylation of lysine residues at histones 3 (H3) and 4 (H4). Depending on the location of the target lysines in the histone tail and the number of methyl groups added, methylation can either activate or inhibit gene expression [14, 24]. Histone phosphorylation is a marker of cell division and has a function in DNA repair, chromatin condensation during division, and regulation of gene expression [14, 25]. The addition of ubiquitin to lysine residues in histones is called ubiquitination and is implicated in DNA repair and control of transcription [14]. Sumoylation is a changeable post-translational adjustment using small ubiquitin-like proteins (SUMO) and has a crucial function in various mechanisms, such as transcription, and cell cycle progression [14, 26].
RNA-based epigenetic mechanisms include long noncoding RNAs (lncRNAs) and microRNAs (miRNAs) [14]. NcRNAs are functional RNAs that do not translate into proteins and play an essential part in epigenetic regulation [14, 16]. The lncRNAs are extremely tissue-specific relative to protein-coding genes [16]. The miRNAs are short (20–22 nucleotides), single-stranded, evolutionarily-conserved ncRNAs that modulate the expression at the post-transcriptional level of more than 50% of cellular genes [13, 14, 27].
Changes in the environment, including temperature, light, and nutritional habits, trigger reversible epigenomic modification that can influence numerous physiological processes [28]. Epigenome-wide association studies (EWAS) provide information about associations between epigenomic perturbations and traits associated with human diseases [29]. EWAS try to evaluate the environmental impact on genetic regulation. The epigenetic variations could explain missing parts of heritability of chronic diseases that have not yet been determined by genome-wide association studies [29].
The primary clock genes show circadian expression in the SCN, and light is one of the key drivers that can reset the rhythm phases. There are several crucial proteins in SCN. Transcription activators are aryl hydrocarbon receptor nuclear translocator-like (ARNTL or BMAL1) and circadian locomotor output cycle caps (CLOCK). Transcription inhibitors are period (PER) and cryptochrome (CRY) [30, 31]. Within 24 h, the entire process of activation and inhibition of gene expression takes place [32, 33]. The circadian system controls gene expression through various mechanisms as a basis of global gene regulation. The first is via E-boxes (promoter and enhancer regulatory elements) of oscillator proteins such as CLOCK, ARNTL, and NPAS2 (neuronal PAS domain protein 2). The second mechanism is using other oscillator proteins such as RORα (retinoic acid receptor-related orphan receptor) and REV-ERBα (or NR1D1, orphan nuclear receptor) via REV-ERB/ROR response element (RRE), which are present in the promoters of specific clock-controlled genes (CCGs) (Figure 1). The third mechanism is the daily chromatin remodeling [2, 19, 34, 35].
Circadian rhythm gene regulation in cardiovascular diseases. ARNTL and CLOCK activate transcription of
The ARNTL-CLOCK heterodimers enhance
Nearly 10% of the transcripts show circadian rhythmicity [19]. Rhythmic expression of crucial metabolic genes is impaired due to clock gene mutations and lead to metabolic disorders [28]. Fasting glucose levels decrease, and insulin sensitivity increases in overexpression of the
Based on circadian rhythms in SCN neurons and peripheral cells, epigenetic mechanisms participate in the formation of circadian rhythms of gene expression [2]. One of the primary circadian genes, CLOCK, has the function of histone acetyltransferase. Chromatin remodeling is an essential underlying mechanism of the clock rhythm and reveals an association between cellular physiology and histone acetylation [2]. ARNTL-CLOCK heterodimer or ARNTL-NPAS2 complex mobilizes HATs and HDACs [28, 44]. To maintain metabolic homeostasis and avoid metabolic disorders, the crosstalk between circadian rhythm and metabolism is necessary [28].
Rapid adaptation of cells to environmental changes is facilitated by epigenetic mechanisms that also offer a link between genes and the environment [1]. The phenotypic variations observed in humans are more significant than genotype variations alone, and changes in epigenetic gene modification explain them [1, 45]. CVDs, such as atherosclerosis, cardiac hypertrophy, myocardial infarction, and heart failure, are associated with epigenetic mechanisms ranging from DNA methylation, histone modification, to ncRNAs [13]. An essential way of developing CVD early in life involves epigenetic changes [12]. The underlying mechanism providing the link between the early life environment and the subsequent CVD risk is epigenetic modifications [12].
The association of methylation with specific genes may be useful in assessing the risk of a disease or in monitoring the response to a particular treatment [14]. In the process of DNA methylation, homocysteine, an amino acid that does not enter into protein composition, is essential [46]. The lack of folate in the diet leads to an increase in plasma homocysteine, which contributes to the rise of S-adenosyl homocysteine. It represses transmethylation reactions and decreases methylation all over the epigenome [1, 46]. In atherogenesis are included homocysteine-induced changes in DNA methylation in smooth muscle vascular cells [1, 47, 48]. Endothelial dysfunction and different aspects of CVD are epigenetically associated with folic acid deficiency [16]. Genomic DNA is hypomethylated in human atherosclerotic lesions [1, 2, 12]. Inflammatory processes involved in the development of atherosclerotic plaques are associated with hypermethylation [1, 49]. There are rhythmic changes in global DNA methylation in human blood, and there is an increased level at night [35]. Changes in circadian rhythm genes methylation were observed in aging mice, but are tissue-dependent [35, 50]. For example, in the stomach of older mice, the methylation of the
The histone code is involved in many aspects of cardiovascular physiology, from endothelial cell responses to hypoxia to recovery from MI [16]. CLOCK has enzymatic properties of histone acetyltransferase (HAT). It performs acetylation at Lys537 of H3 histone and ARNTL, which is necessary for circadian rhythm [1, 9]. CLOCK works in collaboration with other HATs to maintain circadian rhythm in the acetylation state of histones at CCG promoters [6]. HDAC activity has an essential function in defining the intensity of myocardial ischemia, especially after MI [16]. Inhibition of HDAC can promote angiogenesis and reduce myocardial damage after MI [16], such as valproic acid (VPA), which is an HDAC inhibitor [2]. Histone deacetylases, SIRT1 (sirtuin 1), and SIRT6 participate in the histone modification, thus controlling gene expression [35] and providing a molecular connection among metabolism and circadian rhythm [6]. SIRT1 deacetylates regulatory proteins and acts as a rhythm-promoting agent in circadian oscillators [35]. SIRT1 has a unique role in central and peripheral circadian rhythms [35]. The purpose of histone phosphorylation in CVDs is minimal [14], while SUMO proteins influence the activity of several essential factors that are important for cardiac development [14]. There are connections between circadian rhythm regulators, chromatin modifications, and cellular metabolism [1, 52].
Numerous lncRNAs have essential regulatory functions in various CVDs [14]. The miRNAs regulate cholesterol metabolism, oxidative stress, and endothelial dysfunction, diverse cellular processes involved in atherosclerosis [14]. MiRNAs may be relevant regulators of circadian rhythm [1]. Circulating miRNA-145 and miRNA-126 are decreased in patients with coronary artery disease, while miRNA-1, miRNA-499, and miRNA-133b are increased during acute myocardial infarction [13]. All those miRNAs can be biomarkers of CVD.
Circadian rhythms combine metabolic and environmental signals and alter gene expression when adapting the organism to particular circumstances [6]. Many epigenetic regulators in some tissues are controlled in a circadian fashion [19, 53]. The challenge is to determine whether epigenetic variations happen in a rhythmic pattern in tissues included in the CVD development [12, 19]. Epigenetics can contribute to enhancing CVD therapies and finding new markers for CVD screening [16, 54].
DNA methylation is a durable, relatively constant epigenetic change. It involves the covalent attachment of a methyl group to the cytosine [3, 55]. The primary role of DNA methylation is to regulate gene expression by altering the availability of DNA to the transcription factors [3, 13].
DNA methylation links the steady genome and the changing environment. It is an instrument through which environmental changes influence metabolism [7]. Disruption of DNA methylation has been associated with different metabolic diseases such as diabetes [56], obesity, and insulin resistance [57]. Furthermore, the epigenetic mechanisms control circadian rhythm, and circadian disturbance leads to DNA methylation changes of the clock genes [7, 51, 58]. Adiposity, metabolic syndrome, and weight loss are linked to DNA methylation changes of the
DNA methylation is cell- or tissue-specific, but epimutations are not restricted to the affected tissue and may also be observed in peripheral blood [7]. Compared to other genes, the regulatory regions of circadian rhythm genes are plentiful in CpG sites [59, 60]. Patients with coronary artery disease have altered methylation patterns relative to controls [1, 61, 62]. All mentioned supports the assumption that epigenetic variations are associated with an increased CVD risk [1].
Epigenetic alterations of circadian genes are related to obesity and metabolic disorders [17, 63]. A positive association was found between the alteration of the
Global hypomethylation of DNA is present in atherosclerotic lesions [3, 66]. The severity of atherosclerotic lesions correlates with DNA methylation [3, 14, 67, 68]. There are notable variations in DNA methylation after an MI event [69, 70]. DNA methylation status in blood samples is related to CVD [71, 72].
Environmental and behavioral factors, such as inflammation, smoking, physical activity, or stress, can alter the epigenome [63, 73]. Elevated gene expression in the inflammatory pathway is associated with decreased gene methylation [46]. DNA methylation relies on the accessibility of methyl groups obtained from methionine, and the existence of certain nutrients in the food influences epigenetic changes with possible cardiovascular outcomes [46]. Although methylation changes are related to healthy aging, they could be in the background of the development of some diseases, such as CVD [46, 74]. Reduction in global DNA methylation occurs throughout the human lifespan [46].
Post-translational modifications occur at amino acid residues in the amino-terminal regions of histone and cover histone acetylation, methylation, phosphorylation, sumoylation, and ubiquitination. It controls chromatin remodeling and gene expression [3, 23]. Histone acetylation is a sign of transcription activation [75], while histone methylation can both stimulate and inhibit transcription [28, 75]. Post-translational histone modifications control genes coding clock proteins [46, 75]. Epigenetic irregularities are related to different disorders, including atherosclerosis [4, 76].
Histone modifications occur at the CCG promoters in a circadian fashion [4, 44, 77, 78]. The core clock protein, CLOCK, has HAT activity. It revealed the molecular association among epigenetic mechanisms and circadian rhythm [4, 19, 59, 79]. CLOCK acetylates ARNTL, which facilitates CRY-dependent repression [19, 28], and interaction of CRY1 with the ARNTL-CLOCK heterodimer [9]. CLOCK and NPAS2 attract different HATs to the promoter of the
SIRT1 is an NAD + -dependent histone deacetylase [4, 59, 80]. It is needed for rhythmic transcription of some clock genes, such as
Histone modifications, and particularly HDACs, have a significant role in the control of vascular homeostasis. Dysregulation of HDAC could lead to the formation of atherosclerotic lesions [14, 94]. In human carotid arteries, histone methylation and acetylation present recognizable patterns depending on the seriousness of the plaque [46]. Inhibition of HDACs leads to reduced inflammation and atherogenesis [46, 95]. In animal studies, HDAC inhibitors reduce the size of MI and ischemia-reperfusion injury after revascularization [46, 96]. The inhibition of HDAC may improve myocardial recovery and block post-infarction remodeling [46]. Fibrosis after MI was reduced by valproic acid, an HDAC inhibitor [14, 97].
MicroRNAs (miRNAs) are small noncoding RNA molecules that repress the expression of target messenger RNAs [1, 3, 5, 98]. MicroRNA dysregulation is associated with cardiovascular diseases, lipid metabolism, endothelial function, ventricular hypertrophy, and post-infarction dysrhythmias [1, 5].
Oscillating microRNAs, based on external triggers, could affect the expression of target genes in a circadian fashion independently of clock genes [5, 99]. In plasma and serum of CVD patients are observed decreased levels of numerous miRNAs, such as miRNA-126, miRNA-17, miRNA-145, miRNA-92a, and miRNA-155 [3].
MiRNAs control the development of atherosclerosis through their action on endothelial function, plaque progression and rupture, and blood vessel development [46]. MiRNA-126 expressed by endothelial cells serves as an adverse adjuster of vascular inflammation, while miRNA-33 plays a vital role in inhibiting the critical genes implicated in cellular cholesterol export [14, 100]. Some miRNAs target DNMTs and thus regulate the level of DNA methylation in atherosclerotic lesions [14]. MiRNA-148 changes HDL and LDL cholesterol levels in murine models and thus has a vital function in lipid metabolism [46, 101, 102].
MiRNA-24, 29a, and 30a influence the circadian rhythm by regulating the stability and translation of PER1 and PER2 mRNAs [5]. The ARNTL-CLOCK heterodimer controls miRNA-142–3p and, in turn, can target ARNTL [5, 103, 104]. MiRNA-21 is a PER2-dependent miRNA and mediates PER2-obtained cardioprotection [5, 105]. Through cellular stress, PER2-dependent miRNA-21 controls cellular glycolysis. Myocardial ischemia causes activation of pathways aimed at increasing the efficiency of myocardial oxygen [5, 106]. Suppression of miRNA-21 reduces the fibrotic response and enhances cardiac activity [5].
A valuable sign of myocardial cell death is the plasma levels of miRNA-208 [3, 107]. MiRNAs have a function in remodeling after MI, a mechanism closely associated with the expansion of tissue fibrosis [14]. A more sensitive biomarker of acute non-STEM MI is miRNA-499 than cardiac troponin T [46].
MicroRNAs could potentially become new modulators of circadian rhythms and could have a positive effect on cardiovascular physiology [5]. MiRNAs regulate about 60% of all human genes [46]. Therapeutic strategies should target specific microRNAs and thus reduce their capacity to inhibit circadian rhythm components or circadian rhythm output genes [5, 108, 109, 110, 111, 112]. Administration of microRNAs in a circadian-dependent fashion could serve to adapt the impaired circadian system, advance metabolism by enhancing efficient oxygen pathways, and thereby promote cardioprotection from ischemia [5].
The epigenetic variations of an individual change throughout a lifetime and epigenome profiles, instead of genotypes, are reflected in phenotypes in epigenetic epidemiological studies. Therefore, epigenetic modifications are the reason or a result of a pathological condition. Understanding the epigenetic contribution to CVD pathology may help to develop new treatments and diagnostic approaches. Epigenetic biomarkers might be very useful in treatment monitoring and predicting disease outcome. Epigenetic events can potentially be reversibly altered depending on environmental and nutritional factors. Understanding epigenetic mechanisms may identify valuable, novel biomarkers for disease.
The author declares no conflict of interest.
"Open access contributes to scientific excellence and integrity. It opens up research results to wider analysis. It allows research results to be reused for new discoveries. And it enables the multi-disciplinary research that is needed to solve global 21st century problems. Open access connects science with society. It allows the public to engage with research. To go behind the headlines. And look at the scientific evidence. And it enables policy makers to draw on innovative solutions to societal challenges".
\n\nCarlos Moedas, the European Commissioner for Research Science and Innovation at the STM Annual Frankfurt Conference, October 2016.
",metaTitle:"About Open Access",metaDescription:"Open access contributes to scientific excellence and integrity. It opens up research results to wider analysis. It allows research results to be reused for new discoveries. And it enables the multi-disciplinary research that is needed to solve global 21st century problems. Open access connects science with society. It allows the public to engage with research. To go behind the headlines. And look at the scientific evidence. And it enables policy makers to draw on innovative solutions to societal challenges.\n\nCarlos Moedas, the European Commissioner for Research Science and Innovation at the STM Annual Frankfurt Conference, October 2016.",metaKeywords:null,canonicalURL:"about-open-access",contentRaw:'[{"type":"htmlEditorComponent","content":"The Open Access publishing movement started in the early 2000s when academic leaders from around the world participated in the formation of the Budapest Initiative. They developed recommendations for an Open Access publishing process, “which has worked for the past decade to provide the public with unrestricted, free access to scholarly research—much of which is publicly funded. Making the research publicly available to everyone—free of charge and without most copyright and licensing restrictions—will accelerate scientific research efforts and allow authors to reach a larger number of readers” (reference: http://www.budapestopenaccessinitiative.org)
\\n\\nIntechOpen’s co-founders, both scientists themselves, created the company while undertaking research in robotics at Vienna University. Their goal was to spread research freely “for scientists, by scientists’ to the rest of the world via the Open Access publishing model. The company soon became a signatory of the Budapest Initiative, which currently has more than 1000 supporting organizations worldwide, ranging from universities to funders.
\\n\\nAt IntechOpen today, we are still as committed to working with organizations and people who care about scientific discovery, to putting the academic needs of the scientific community first, and to providing an Open Access environment where scientists can maximize their contribution to scientific advancement. By opening up access to the world’s scientific research articles and book chapters, we aim to facilitate greater opportunity for collaboration, scientific discovery and progress. We subscribe wholeheartedly to the Open Access definition:
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\\n\\nLicense
\\n\\nBook chapters published in edited volumes are distributed under the Creative Commons Attribution 3.0 Unported License (CC BY 3.0). IntechOpen upholds a very flexible Copyright Policy. There is no copyright transfer to the publisher and Authors retain exclusive copyright to their work. All Monographs/Compacts are distributed under the Creative Commons Attribution-NonCommercial 4.0 International (CC BY-NC 4.0). Read more
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\\n\\nAll scientific works are Peer Reviewed prior to publishing. Read more
\\n\\nOA Publishing Fees
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\\n\\nOpen Science is transparent and accessible knowledge that is shared and developed through collaborative networks.
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The Open Access publishing movement started in the early 2000s when academic leaders from around the world participated in the formation of the Budapest Initiative. They developed recommendations for an Open Access publishing process, “which has worked for the past decade to provide the public with unrestricted, free access to scholarly research—much of which is publicly funded. Making the research publicly available to everyone—free of charge and without most copyright and licensing restrictions—will accelerate scientific research efforts and allow authors to reach a larger number of readers” (reference: http://www.budapestopenaccessinitiative.org)
\n\nIntechOpen’s co-founders, both scientists themselves, created the company while undertaking research in robotics at Vienna University. Their goal was to spread research freely “for scientists, by scientists’ to the rest of the world via the Open Access publishing model. The company soon became a signatory of the Budapest Initiative, which currently has more than 1000 supporting organizations worldwide, ranging from universities to funders.
\n\nAt IntechOpen today, we are still as committed to working with organizations and people who care about scientific discovery, to putting the academic needs of the scientific community first, and to providing an Open Access environment where scientists can maximize their contribution to scientific advancement. By opening up access to the world’s scientific research articles and book chapters, we aim to facilitate greater opportunity for collaboration, scientific discovery and progress. We subscribe wholeheartedly to the Open Access definition:
\n\n“By “open access” to [peer-reviewed research literature], we mean its free availability on the public internet, permitting any users to read, download, copy, distribute, print, search, or link to the full texts of these articles, crawl them for indexing, pass them as data to software, or use them for any other lawful purpose, without financial, legal, or technical barriers other than those inseparable from gaining access to the internet itself. The only constraint on reproduction and distribution, and the only role for copyright in this domain, should be to give authors control over the integrity of their work and the right to be properly acknowledged and cited” (reference: http://www.budapestopenaccessinitiative.org)
\n\nOAI-PMH
\n\nAs a firm believer in the wider dissemination of knowledge, IntechOpen supports the Open Access Initiative Protocol for Metadata Harvesting (OAI-PMH Version 2.0). Read more
\n\nLicense
\n\nBook chapters published in edited volumes are distributed under the Creative Commons Attribution 3.0 Unported License (CC BY 3.0). IntechOpen upholds a very flexible Copyright Policy. There is no copyright transfer to the publisher and Authors retain exclusive copyright to their work. All Monographs/Compacts are distributed under the Creative Commons Attribution-NonCommercial 4.0 International (CC BY-NC 4.0). Read more
\n\nPeer Review Policies
\n\nAll scientific works are Peer Reviewed prior to publishing. Read more
\n\nOA Publishing Fees
\n\nThe Open Access publishing model employed by IntechOpen eliminates subscription charges and pay-per-view fees, enabling readers to access research at no cost. In order to sustain operations and keep our publications freely accessible we levy an Open Access Publishing Fee for manuscripts, which helps us cover the costs of editorial work and the production of books. Read more
\n\nDigital Archiving Policy
\n\nIntechOpen is committed to ensuring the long-term preservation and the availability of all scholarly research we publish. We employ a variety of means to enable us to deliver on our commitments to the scientific community. Apart from preservation by the Croatian National Library (for publications prior to April 18, 2018) and the British Library (for publications after April 18, 2018), our entire catalogue is preserved in the CLOCKSS archive.
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\n\nOpen Science refers to doing traditional science with more transparency involved at various stages, for example by openly sharing code and data. It implies a growing set of practices - within different disciplines - aiming at:
\n\nWe aim at improving the quality and availability of scholarly communication by promoting and practicing:
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The preliminary objectives of the study are to understand and develop the evidence-based tools and interventions for the control and prevention of malaria in different sites of the INDIA. Alongside, with the help of next-generation genomics study, the team has studied the antimalarial drug resistance in India. Further, he has extended his research in the development of Humanized mice for the study of liver-stage malaria and identification of molecular marker(s) for the Artemisinin resistance. At present, his research focuses on understanding the role of B cells in the activation of CD8+ T cells in malaria. Received the CSIR-SRF (Senior Research Fellow) award-2018, FIMSA (Federation of Immunological Societies of Asia-Oceania) Travel Bursary award to attend the IUIS-IIS-FIMSA Immunology course-2019',institutionString:"Nirma University",institution:{name:"Nirma University",country:{name:"India"}}},{id:"334383",title:"Ph.D.",name:"Simone",middleName:"Ulrich",surname:"Ulrich Picoli",slug:"simone-ulrich-picoli",fullName:"Simone Ulrich Picoli",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/334383/images/15919_n.jpg",biography:"Graduated in Pharmacy from Universidade Luterana do Brasil (1999), Master in Agricultural and Environmental Microbiology from Federal University of Rio Grande do Sul (2002), Specialization in Clinical Microbiology from Universidade de São Paulo, USP (2007) and PhD in Sciences in Gastroenterology and Hepatology (2012). She is currently an Adjunct Professor at Feevale University in Medicine and Biomedicine courses and a permanent professor of the Academic Master\\'s Degree in Virology. She has experience in the field of Microbiology, with an emphasis on Bacteriology, working mainly on the following topics: bacteriophages, bacterial resistance, clinical microbiology and food microbiology.",institutionString:null,institution:{name:"Universidade Feevale",country:{name:"Brazil"}}},{id:"229220",title:"Dr.",name:"Amjad",middleName:"Islam",surname:"Aqib",slug:"amjad-aqib",fullName:"Amjad Aqib",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/229220/images/system/229220.png",biography:"Dr. Amjad Islam Aqib obtained a DVM and MSc (Hons) from University of Agriculture Faisalabad (UAF), Pakistan, and a PhD from the University of Veterinary and Animal Sciences Lahore, Pakistan. Dr. Aqib joined the Department of Clinical Medicine and Surgery at UAF for one year as an assistant professor where he developed a research laboratory designated for pathogenic bacteria. Since 2018, he has been Assistant Professor/Officer in-charge, Department of Medicine, Manager Research Operations and Development-ORIC, and President One Health Club at Cholistan University of Veterinary and Animal Sciences, Bahawalpur, Pakistan. He has nearly 100 publications to his credit. His research interests include epidemiological patterns and molecular analysis of antimicrobial resistance and modulation and vaccine development against animal pathogens of public health concern.",institutionString:"Cholistan University of Veterinary and Animal Sciences",institution:null},{id:"62900",title:"Prof.",name:"Fethi",middleName:null,surname:"Derbel",slug:"fethi-derbel",fullName:"Fethi Derbel",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/62900/images/system/62900.jpeg",biography:"Professor Fethi Derbel was born in 1960 in Tunisia. He received his medical degree from the Sousse Faculty of Medicine at Sousse, University of Sousse, Tunisia. He completed his surgical residency in General Surgery at the University Hospital Farhat Hached of Sousse and was a member of the Unit of Liver Transplantation in the University of Rennes, France. He then worked in the Department of Surgery at the Sahloul University Hospital in Sousse. Professor Derbel is presently working at the Clinique les Oliviers, Sousse, Tunisia. His hospital activities are mostly concerned with laparoscopic, colorectal, pancreatic, hepatobiliary, and gastric surgery. He is also very interested in hernia surgery and performs ventral hernia repairs and inguinal hernia repairs. He has been a member of the GREPA and Tunisian Hernia Society (THS). During his residency, he managed patients suffering from diabetic foot, and he was very interested in this pathology. For this reason, he decided to coordinate a book project dealing with the diabetic foot. Professor Derbel has published many articles in journals and collaborates intensively with IntechOpen Access Publisher as an editor.",institutionString:"Clinique les Oliviers",institution:null},{id:"300144",title:"Dr.",name:"Meriem",middleName:null,surname:"Braiki",slug:"meriem-braiki",fullName:"Meriem Braiki",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/300144/images/system/300144.jpg",biography:"Dr. Meriem Braiki is a specialist in pediatric surgeon from Tunisia. She was born in 1985. She received her medical degree from the University of Medicine at Sousse, Tunisia. She achieved her surgical residency training periods in Pediatric Surgery departments at University Hospitals in Monastir, Tunis and France.\r\nShe is currently working at the Pediatric surgery department, Sidi Bouzid Hospital, Tunisia. Her hospital activities are mostly concerned with laparoscopic, parietal, urological and digestive surgery. She has published several articles in diffrent journals.",institutionString:"Sidi Bouzid Regional Hospital",institution:null},{id:"229481",title:"Dr.",name:"Erika M.",middleName:"Martins",surname:"de Carvalho",slug:"erika-m.-de-carvalho",fullName:"Erika M. de Carvalho",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/229481/images/6397_n.jpg",biography:null,institutionString:null,institution:{name:"Oswaldo Cruz Foundation",country:{name:"Brazil"}}},{id:"186537",title:"Prof.",name:"Tonay",middleName:null,surname:"Inceboz",slug:"tonay-inceboz",fullName:"Tonay Inceboz",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/186537/images/system/186537.jfif",biography:"I was graduated from Ege University of Medical Faculty (Turkey) in 1988 and completed his Med. PhD degree in Medical Parasitology at the same university. I became an Associate Professor in 2008 and Professor in 2014. I am currently working as a Professor at the Department of Medical Parasitology at Dokuz Eylul University, Izmir, Turkey.\n\nI have given many lectures, presentations in different academic meetings. I have more than 60 articles in peer-reviewed journals, 18 book chapters, 1 book editorship.\n\nMy research interests are Echinococcus granulosus, Echinococcus multilocularis (diagnosis, life cycle, in vitro and in vivo cultivation), and Trichomonas vaginalis (diagnosis, PCR, and in vitro cultivation).",institutionString:"Dokuz Eylül University",institution:{name:"Dokuz Eylül University",country:{name:"Turkey"}}},{id:"71812",title:"Prof.",name:"Hanem Fathy",middleName:"Fathy",surname:"Khater",slug:"hanem-fathy-khater",fullName:"Hanem Fathy Khater",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/71812/images/1167_n.jpg",biography:"Prof. Khater is a Professor of Parasitology at Benha University, Egypt. She studied for her doctoral degree, at the Department of Entomology, College of Agriculture, Food and Natural Resources, University of Missouri, Columbia, USA. She has completed her Ph.D. degrees in Parasitology in Egypt, from where she got the award for “the best scientific Ph.D. dissertation”. She worked at the School of Biological Sciences, Bristol, England, the UK in controlling insects of medical and veterinary importance as a grant from Newton Mosharafa, the British Council. Her research is focused on searching of pesticides against mosquitoes, house flies, lice, green bottle fly, camel nasal botfly, soft and hard ticks, mites, and the diamondback moth as well as control of several parasites using safe and natural materials to avoid drug resistances and environmental contamination.",institutionString:null,institution:{name:"Banha University",country:{name:"Egypt"}}},{id:"99780",title:"Prof.",name:"Omolade",middleName:"Olayinka",surname:"Okwa",slug:"omolade-okwa",fullName:"Omolade Okwa",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/99780/images/system/99780.jpg",biography:"Omolade Olayinka Okwa is presently a Professor of Parasitology at Lagos State University, Nigeria. She has a PhD in Parasitology (1997), an MSc in Cellular Parasitology (1992), and a BSc (Hons) Zoology (1990) all from the University of Ibadan, Nigeria. She teaches parasitology at the undergraduate and postgraduate levels. She was a recipient of a Commonwealth fellowship supported by British Council tenable at the Centre for Entomology and Parasitology (CAEP), Keele University, United Kingdom between 2004 and 2005. She was awarded an Honorary Visiting Research Fellow at the same university from 2005 to 2007. \nShe has been an external examiner to the Department of Veterinary Microbiology and Parasitology, University of Ibadan, MSc programme between 2010 and 2012. She is a member of the Nigerian Society of Experimental Biology (NISEB), Parasitology and Public Health Society of Nigeria (PPSN), Science Association of Nigeria (SAN), Zoological Society of Nigeria (ZSN), and is Vice Chairperson of the Organisation of Women in Science (OWSG), LASU chapter. She served as Head of Department of Zoology and Environmental Biology, Lagos State University from 2007 to 2010 and 2014 to 2016. She is a reviewer for several local and international journals such as Unilag Journal of Science, Libyan Journal of Medicine, Journal of Medicine and Medical Sciences, and Annual Research and Review in Science. \nShe has authored 45 scientific research publications in local and international journals, 8 scientific reviews, 4 books, and 3 book chapters, which includes the books “Malaria Parasites” and “Malaria” which are IntechOpen access publications.",institutionString:"Lagos State University",institution:{name:"Lagos State University",country:{name:"Nigeria"}}},{id:"273100",title:"Dr.",name:"Vijay",middleName:null,surname:"Gayam",slug:"vijay-gayam",fullName:"Vijay Gayam",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/273100/images/system/273100.jpeg",biography:"Dr. Vijay Bhaskar Reddy Gayam is currently practicing as an internist at Interfaith Medical Center in Brooklyn, New York, USA. He is also a Clinical Assistant Professor at the SUNY Downstate University Hospital and Adjunct Professor of Medicine at the American University of Antigua. He is a holder of an M.B.B.S. degree bestowed to him by Osmania Medical College and received his M.D. at Interfaith Medical Center. His career goals thus far have heavily focused on direct patient care, medical education, and clinical research. He currently serves in two leadership capacities; Assistant Program Director of Medicine at Interfaith Medical Center and as a Councilor for the American\r\nFederation for Medical Research. As a true academician and researcher, he has more than 50 papers indexed in international peer-reviewed journals. He has also presented numerous papers in multiple national and international scientific conferences. His areas of research interest include general internal medicine, gastroenterology and hepatology. He serves as an editor, editorial board member and reviewer for multiple international journals. His research on Hepatitis C has been very successful and has led to multiple research awards, including the 'Equity in Prevention and Treatment Award” from the New York Department of Health Viral Hepatitis Symposium (2018) and the 'Presidential Poster Award” awarded to him by the American College of Gastroenterology (2018). He was also awarded 'Outstanding Clinician in General Medicine” by Venus International Foundation for his extensive research expertise and services, perform over and above the standard expected in the advancement of healthcare, patient safety and quality of care.",institutionString:"Interfaith Medical Center",institution:{name:"Interfaith Medical Center",country:{name:"United States of America"}}},{id:"93517",title:"Dr.",name:"Clement",middleName:"Adebajo",surname:"Meseko",slug:"clement-meseko",fullName:"Clement Meseko",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/93517/images/system/93517.jpg",biography:"Dr. Clement Meseko obtained DVM and PhD degree in Veterinary Medicine and Virology respectively. He has worked for over 20 years in both private and public sectors including the academia, contributing to knowledge and control of infectious disease. Through the application of epidemiological skill, classical and molecular virological skills, he investigates viruses of economic and public health importance for the mitigation of the negative impact on people, animal and the environment in the context of Onehealth. \r\nDr. Meseko’s field experience on animal and zoonotic diseases and pathogen dynamics at the human-animal interface over the years shaped his carrier in research and scientific inquiries. He has been part of the investigation of Highly Pathogenic Avian Influenza incursions in sub Saharan Africa and monitors swine Influenza (Pandemic influenza Virus) agro-ecology and potential for interspecies transmission. He has authored and reviewed a number of journal articles and book chapters.",institutionString:"National Veterinary Research Institute",institution:{name:"National Veterinary Research Institute",country:{name:"Nigeria"}}},{id:"158026",title:"Prof.",name:"Shailendra K.",middleName:null,surname:"Saxena",slug:"shailendra-k.-saxena",fullName:"Shailendra K. Saxena",position:null,profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRET3QAO/Profile_Picture_2022-05-10T10:10:26.jpeg",biography:"Professor Dr. Shailendra K. Saxena is a vice dean and professor at King George's Medical University, Lucknow, India. His research interests involve understanding the molecular mechanisms of host defense during human viral infections and developing new predictive, preventive, and therapeutic strategies for them using Japanese encephalitis virus (JEV), HIV, and emerging viruses as a model via stem cell and cell culture technologies. His research work has been published in various high-impact factor journals (Science, PNAS, Nature Medicine) with a high number of citations. He has received many awards and honors in India and abroad including various Young Scientist Awards, BBSRC India Partnering Award, and Dr. JC Bose National Award of Department of Biotechnology, Min. of Science and Technology, Govt. of India. Dr. Saxena is a fellow of various international societies/academies including the Royal College of Pathologists, United Kingdom; Royal Society of Medicine, London; Royal Society of Biology, United Kingdom; Royal Society of Chemistry, London; and Academy of Translational Medicine Professionals, Austria. He was named a Global Leader in Science by The Scientist. He is also an international opinion leader/expert in vaccination for Japanese encephalitis by IPIC (UK).",institutionString:"King George's Medical University",institution:{name:"King George's Medical University",country:{name:"India"}}},{id:"94928",title:"Dr.",name:"Takuo",middleName:null,surname:"Mizukami",slug:"takuo-mizukami",fullName:"Takuo Mizukami",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/94928/images/6402_n.jpg",biography:null,institutionString:null,institution:{name:"National Institute of Infectious Diseases",country:{name:"Japan"}}},{id:"233433",title:"Dr.",name:"Yulia",middleName:null,surname:"Desheva",slug:"yulia-desheva",fullName:"Yulia Desheva",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/233433/images/system/233433.png",biography:"Dr. Yulia Desheva is a leading researcher at the Institute of Experimental Medicine, St. Petersburg, Russia. She is a professor in the Stomatology Faculty, St. Petersburg State University. She has expertise in the development and evaluation of a wide range of live mucosal vaccines against influenza and bacterial complications. Her research interests include immunity against influenza and COVID-19 and the development of immunization schemes for high-risk individuals.",institutionString:'Federal State Budgetary Scientific Institution "Institute of Experimental Medicine"',institution:null},{id:"238958",title:"Mr.",name:"Atamjit",middleName:null,surname:"Singh",slug:"atamjit-singh",fullName:"Atamjit Singh",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/238958/images/6575_n.jpg",biography:null,institutionString:null,institution:null},{id:"333753",title:"Dr.",name:"Rais",middleName:null,surname:"Ahmed",slug:"rais-ahmed",fullName:"Rais Ahmed",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/333753/images/20168_n.jpg",biography:null,institutionString:null,institution:null},{id:"252058",title:"M.Sc.",name:"Juan",middleName:null,surname:"Sulca",slug:"juan-sulca",fullName:"Juan Sulca",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/252058/images/12834_n.jpg",biography:null,institutionString:null,institution:null},{id:"191392",title:"Dr.",name:"Marimuthu",middleName:null,surname:"Govindarajan",slug:"marimuthu-govindarajan",fullName:"Marimuthu Govindarajan",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/191392/images/5828_n.jpg",biography:"Dr. M. Govindarajan completed his BSc degree in Zoology at Government Arts College (Autonomous), Kumbakonam, and MSc, MPhil, and PhD degrees at Annamalai University, Annamalai Nagar, Tamil Nadu, India. He is serving as an assistant professor at the Department of Zoology, Annamalai University. His research interests include isolation, identification, and characterization of biologically active molecules from plants and microbes. He has identified more than 20 pure compounds with high mosquitocidal activity and also conducted high-quality research on photochemistry and nanosynthesis. He has published more than 150 studies in journals with impact factor and 2 books in Lambert Academic Publishing, Germany. He serves as an editorial board member in various national and international scientific journals.",institutionString:null,institution:null},{id:"274660",title:"Dr.",name:"Damodar",middleName:null,surname:"Paudel",slug:"damodar-paudel",fullName:"Damodar Paudel",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/274660/images/8176_n.jpg",biography:"I am DrDamodar Paudel,currently working as consultant Physician in Nepal police Hospital.",institutionString:null,institution:null},{id:"241562",title:"Dr.",name:"Melvin",middleName:null,surname:"Sanicas",slug:"melvin-sanicas",fullName:"Melvin Sanicas",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/241562/images/6699_n.jpg",biography:null,institutionString:null,institution:null},{id:"337446",title:"Dr.",name:"Maria",middleName:null,surname:"Zavala-Colon",slug:"maria-zavala-colon",fullName:"Maria Zavala-Colon",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"University of Puerto Rico, Medical Sciences Campus",country:{name:"United States of America"}}},{id:"338856",title:"Mrs.",name:"Nur Alvira",middleName:null,surname:"Pascawati",slug:"nur-alvira-pascawati",fullName:"Nur Alvira Pascawati",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"Universitas Respati Yogyakarta",country:{name:"Indonesia"}}},{id:"441116",title:"Dr.",name:"Jovanka M.",middleName:null,surname:"Voyich",slug:"jovanka-m.-voyich",fullName:"Jovanka M. 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Animals need to receive a properly balanced diet. One of the new challenges we are now faced with is sustainable animal diets (STAND) that involve the 3 P’s (People, Planet, and Profitability). We must develop animal feed that does not compete with human food, use antibiotics, and explore new growth promoters options, such as plant extracts or compounds that promote feed efficiency (e.g., monensin, oils, enzymes, probiotics). These new feed options must also be environmentally friendly, reducing the Carbon footprint, CH4, N, and P emissions to the environment, with an adequate formulation of nutrients.",coverUrl:"https://cdn.intechopen.com/series_topics/covers/20.jpg",hasOnlineFirst:!0,hasPublishedBooks:!0,annualVolume:11416,editor:{id:"175967",title:"Dr.",name:"Manuel",middleName:null,surname:"Gonzalez Ronquillo",slug:"manuel-gonzalez-ronquillo",fullName:"Manuel Gonzalez Ronquillo",profilePictureURL:"https://mts.intechopen.com/storage/users/175967/images/system/175967.png",biography:"Dr. Manuel González Ronquillo obtained his doctorate degree from the University of Zaragoza, Spain, in 2001. He is a research professor at the Faculty of Veterinary Medicine and Animal Husbandry, Autonomous University of the State of Mexico. He is also a level-2 researcher. He received a Fulbright-Garcia Robles fellowship for a postdoctoral stay at the US Dairy Forage Research Center, Madison, Wisconsin, USA in 2008–2009. He received grants from Alianza del Pacifico for a stay at the University of Magallanes, Chile, in 2014, and from Consejo Nacional de Ciencia y Tecnología (CONACyT) to work in the Food and Agriculture Organization’s Animal Production and Health Division (AGA), Rome, Italy, in 2014–2015. He has collaborated with researchers from different countries and published ninety-eight journal articles. He teaches various degree courses in zootechnics, sheep production, and agricultural sciences and natural resources.\n\nDr. Ronquillo’s research focuses on the evaluation of sustainable animal diets (StAnD), using native resources of the region, decreasing carbon footprint, and applying meta-analysis and mathematical models for a better understanding of animal production.",institutionString:null,institution:{name:"Universidad Autónoma del Estado de México",institutionURL:null,country:{name:"Mexico"}}},editorTwo:null,editorThree:null,series:{id:"13",title:"Veterinary Medicine and Science",doi:"10.5772/intechopen.73681",issn:"2632-0517"},editorialBoard:[{id:"175762",title:"Dr.",name:"Alfredo J.",middleName:null,surname:"Escribano",slug:"alfredo-j.-escribano",fullName:"Alfredo J. 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