More than half of the publishers listed alongside IntechOpen (18 out of 30) are Social Science and Humanities publishers. IntechOpen is an exception to this as a leader in not only Open Access content but Open Access content across all scientific disciplines, including Physical Sciences, Engineering and Technology, Health Sciences, Life Science, and Social Sciences and Humanities.
\\n\\n
Our breakdown of titles published demonstrates this with 47% PET, 31% HS, 18% LS, and 4% SSH books published.
\\n\\n
“Even though ItechOpen has shown the potential of sci-tech books using an OA approach,” other publishers “have shown little interest in OA books.”
\\n\\n
Additionally, each book published by IntechOpen contains original content and research findings.
\\n\\n
We are honored to be among such prestigious publishers and we hope to continue to spearhead that growth in our quest to promote Open Access as a true pioneer in OA book publishing.
Simba Information has released its Open Access Book Publishing 2020 - 2024 report and has again identified IntechOpen as the world’s largest Open Access book publisher by title count.
\n\n
Simba Information is a leading provider for market intelligence and forecasts in the media and publishing industry. The report, published every year, provides an overview and financial outlook for the global professional e-book publishing market.
\n\n
IntechOpen, De Gruyter, and Frontiers are the largest OA book publishers by title count, with IntechOpen coming in at first place with 5,101 OA books published, a good 1,782 titles ahead of the nearest competitor.
\n\n
Since the first Open Access Book Publishing report published in 2016, IntechOpen has held the top stop each year.
\n\n\n\n
More than half of the publishers listed alongside IntechOpen (18 out of 30) are Social Science and Humanities publishers. IntechOpen is an exception to this as a leader in not only Open Access content but Open Access content across all scientific disciplines, including Physical Sciences, Engineering and Technology, Health Sciences, Life Science, and Social Sciences and Humanities.
\n\n
Our breakdown of titles published demonstrates this with 47% PET, 31% HS, 18% LS, and 4% SSH books published.
\n\n
“Even though ItechOpen has shown the potential of sci-tech books using an OA approach,” other publishers “have shown little interest in OA books.”
\n\n
Additionally, each book published by IntechOpen contains original content and research findings.
\n\n
We are honored to be among such prestigious publishers and we hope to continue to spearhead that growth in our quest to promote Open Access as a true pioneer in OA book publishing.
\n\n
\n\n
\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:"1704",leadTitle:null,fullTitle:"Future Aeronautical Communications",title:"Future Aeronautical Communications",subtitle:null,reviewType:"peer-reviewed",abstract:"There are well-founded concerns that current air transportation systems will not be able to cope with their expected growth. 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Today's and tomorrow's problems / methods in the field of aeronautical communications are treated: current trends are identified; IPv6 aeronautical network aspect are covered; challenges for the satellite component are illustrated; AeroMACS and LDACS as future data links are investigated and visions for aeronautical communications are formulated.",isbn:null,printIsbn:"978-953-307-625-6",pdfIsbn:"978-953-51-6061-8",doi:"10.5772/2147",price:139,priceEur:155,priceUsd:179,slug:"future-aeronautical-communications",numberOfPages:394,isOpenForSubmission:!1,isInWos:1,isInBkci:!1,hash:"0b8e37964820587b229361f22d299b29",bookSignature:"Simon Plass",publishedDate:"September 26th 2011",coverURL:"https://cdn.intechopen.com/books/images_new/1704.jpg",numberOfDownloads:59428,numberOfWosCitations:34,numberOfCrossrefCitations:42,numberOfCrossrefCitationsByBook:4,numberOfDimensionsCitations:75,numberOfDimensionsCitationsByBook:4,hasAltmetrics:1,numberOfTotalCitations:151,isAvailableForWebshopOrdering:!0,dateEndFirstStepPublish:"February 17th 2011",dateEndSecondStepPublish:"February 17th 2011",dateEndThirdStepPublish:"May 20th 2011",dateEndFourthStepPublish:"June 21st 2011",dateEndFifthStepPublish:"October 21st 2011",currentStepOfPublishingProcess:5,indexedIn:"1,2,3,4,5,6,7",editedByType:"Edited by",kuFlag:!1,featuredMarkup:null,editors:[{id:"72892",title:"Dr.",name:"Simon",middleName:null,surname:"Plass",slug:"simon-plass",fullName:"Simon Plass",profilePictureURL:"https://mts.intechopen.com/storage/users/72892/images/system/72892.jpg",biography:"Dr. Simon Plass received the Dr.Ing. degree (Ph.D.) in electrical engineering from the University of Ulm, Germany in 2008. 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1. Introduction
In last decades, in effect of high price of fossil fuel, environmental pollution due to fossil fuel utilization and greenhouse effect, renewable energy resources are considered as an alternative energy resource to the World’s excessive energy demand. Nowadays, different technologies are utilized to energy generation from hydro power, fuel cell and hydrogen, biomass, geothermal, solar thermal, photovoltaic and wind, while the technology for converting ocean powers are still in infancy. The aim of this chapter is to introduce potential renewable power sources of ocean, mostly ocean wave power, as well as available technologies for extracting wave power. Due to high energy amount available in ocean, the issue has a strong importance to investigate. Furthermore there are variety of technologies that are developed for harnessing wave power each of which has an individual mechanism. Harvesting ocean wave power and converting to electrical power is a challenge for marine, mechanical, electrical and control engineers and we hope to give essential information about ocean wave, methods of energy extracting from wave and related electrical equipment.
1.1. Ocean
The oceans contain 97.2% of total world water which are covering 71% of Earth’s surface [1]. Also the oceans intrinsically are couple with atmosphere via air-water interface and they exchange heat, moisture, momentum and trace constituents by means of air-water interface [2]. The fundamental processes that transfer energy from atmosphere to ocean are energy input to ocean by wind and net surface heat flux [3]. Furthermore, ocean absorbs heat of geothermal energy via geothermal vent in ocean bed. So that, oceans are vigorous and ubiquitous sources of renewable energy which contain 93100 TWh of energy annually [4]. Energy in oceans comes in various forms such as tides, surface wave, thermal gradient, ocean circulation and salinity gradients. It is apparent that ocean with its high amount of energy and global realm on Earth surface can be appropriately utilized for generating electric power. To date, diverse technologies has been developed for extracting different energy forms of ocean most of which are in infancy stage and there is a challenging road before scientists and engineers to generates electricity from ocean in a cost-effective manner.
1.2. Ocean waves
The most potent form of ocean energy is ocean wave. According to the International Energy Agency report, It is estimated that ocean waves have approximately 10000-15000 TWh of energy annually [4], also last researches clarified that 2.11±0.05TW (to 95% confidence) of ocean waves power facing total coastlines of the world [5].
Ocean wave is created by wind, as a byproduct of the solar energy. As solar energy is converted to wind energy, the time-averaged power flow is spatially concentrated, from an intensity of typically 0.1–0.3 kW/m2 horizontal surface of the earth to 0.5 kW/m2 envisaged area perpendicular to wind direction. As wind energy is converted to wave energy, even more spatial concentration takes place. Just below the ocean surface, average power flow intensity is typically 2–3 kW/m2of envisaged area perpendicular to direction of wave propagation [6]. Because of increase in power intensity, the wave energy is more persistent than wind energy or solar energy. In addition to wind, passing ships and subsea earthquakes generate waves while their contribution in total generated ocean wave power is negligible in comparison to wind.
When wind generates disturbance on ocean surface, gravity or surface tension act as restoring forces that tend to drive water toward its equilibrium state consequently ocean waves manifest themselves. Ocean waves can travel thousands of kilometers with little energy loss. When a wave is propagating, the water particles are not traveling, in fact they move clockwise around a small ellipse with the same period as the progressive wave which drives the motion [7]. The ellipse has its axes vertical and horizontal. By approaching to the seabed, the ellipses become progressively thinner in the vertical direction. At the sea bed, the water particles slip back and forth horizontally. Since the entire particle paths are closed loops, there is no net mass transport by the wave. Equation of water particles’ pathway while taking part in a gravity wave motion is as follow;
Where AI is amplitude of wave, X0 and Z0 are the initial position of water particle in x (wave propagation direction) and z (gravity acceleration direction) directions in Cartesian coordinates respectively, h is ocean depth, ω is angular velocity of ocean wave harmonics, g is gravity acceleration and k is wave number which is achieved from dispersion relation. According to the Eq. (1), by approaching to the sea bed Z0→−h so that sinh(Z0+h) and Z1 tend to zero and water particle displacement abates in vertical direction.
Another important characteristic of gravity waves is propagation velocity of ocean waves. The importance is due to intrinsic relation of ocean wave power with group propagation velocity. Angular velocity for different harmonics of ocean waves is calculated according to the Eq. (2), so called dispersion relation, and phase velocity is achieved from Eq.(3);
ω2=gktanh(kh)E2
vp=ωk=gλ2πtan(2πhλ)E3
In above equation, vp is phase velocity of ocean wave harmonics and λ is wavelength of ocean wave. As Eq. (3), the phase velocity depends on ocean depth so that a distinct wave propagates in different depth of ocean with different velocities. There are two possible values for phase velocity. In shallow water, where ocean depth is significantly less than wavelength (h≪λ), the phase velocity is;
vp=ghE4
And phase velocity in deep water, where ocean depth is more than wave length (h≫λ), is as follow;
vp=gλ2πE5
With respect to Eq. (4), in shallow water, wave is not dispersive and various harmonics of wave propagates with same velocity, while in deep water, according to Eq. (5), waves are dispersive. It means wave with different wavelength propagate with different velocities proportional to their wavelength.
Total power that is carried by one harmonic of wave in unit length of wave crest, called wave energy transport, is as below equation;
J=ρg2AI24ω(1+2khsinh(2kh))tan(kh)=ρgAI22vgE6
While, ρis density of ocean water and vg is group velocity of wave that is equal to phase velocity in shallow watervg=vp=gh and in deep water is equal to half of phase velocity 2vg=vp=gλ/2π. According to different wave propagation velocity in deep and shallow waters and related energy transport by wave in these environments and by considering various methods of extracting wave power by different devices and related commercial, installation and maintaining issues, ocean waves study is divided to three different areas called; shoreline, near-shore and off-shore.
Off-shore is a location of ocean in where depth is more than 40 meters. In this location ocean waves have the most power.
Near-shore is location with ocean depth of 10-30 meters and typically has a distance of 0.5-2Km from coastline. In near-shore, seabed fraction is the major source of incident wave power reduction. For instance, in location with ocean depth of 10 meters, different harmonics of ocean waves losses 2-10% of their total power [8].
Shoreline is the location of ocean where depth is less than 10 m. In this location most of the wave power is declined due to seabed fraction and wave breaking.
Not only amount of wave power is various in off-shore and in-shore (shoreline and near-shore) but also ocean wave power is not uniformly separate in all oceans. Fig. 1 illustrates global distribution of wave power density [5]. The arrows on the plot show the mean best wave propagation direction. This figure represents that most of wave power is concentrated in western part of continents which is due to west to east winds. The highest levels in the Northern Hemisphere are off the west coast of the British Isles, Iceland and Greenland, with somewhat lower energy levels in the Pacific off the western seaboard of the US and Canada in Southern Hemisphere Chile, South Africa and the entire south and south west coasts of Australia and New Zealand.
Figure 1.
Global annual mean wave power density and annual mean best direction (arrow) [5].
In other point of view, ocean wave power is denser between 40º-60º latitudes in both Northern and Southern hemisphere. Stephen Barstow et al. represented relevance of annual mean ocean wave power density to latitude as Fig. 2. It is shown that ocean wave power is mostly travelling between 40º-60º latitudes [9].
Figure 2.
Global annual mean wave power density with respect to latitude [9].
Ocean waves are variable in different time scales. The average wave energy for a winter month can be 5–10 times the mean value for a summer month. The wave energy can vary 10 times from one week to the next. The wave energy during one storm can be five times higher than the mean value for the week the storm occurs. Wave energy in a wave group can be up to 50 times the wave energy between wave groups [10]. In Fig. 3, Monthly mean ocean wave power is plotted for different months of year. According to this figure ocean wave power in both Hemispheres is significantly higher in winter season in comparison to summer. Also seasonal variation of wave power in southern Hemisphere is lower than northern one.
Figure 3.
Monthly mean wave power for Northern and southern Hemispheres [5].
1.3. Wave measurement and prediction
Ocean waves are variable in different time scales. Not only wave elevation and wave length (wave power) but also wave propagation direction varies with time. These detailed statistics are important for designing and controlling of particular Wave Energy Convertor (WEC). In most of cases, WECs extract wave power with oscillation in special directions and these WECs absorb maximum power whereby are adjusted in the resonance frequency, a restricted frequency span that WECs oscillation frequency is equal to exciting wave frequency. Implementing upcoming characteristic parameters of ocean wave (amplitude, propagation direction and wave length or period) has a significant impact on capture width of WECs. This information can be used for generator speed control. In all WECs, rotating or linear electric generator is utilized for generating electrical power, implementing information of upcoming wave can be used for speed control of generator and adjusting system in resonance frequency [11]. Briefly, measurement and anticipation of upcoming ocean wave parameters play a significant role in controlling of a WEC. To date, there are various instruments for measuring and predicting ocean wave some of which are described as follow;
1.3.1. Buoy
Buoys are the oldest method for measuring wave parameters. Buoys can measure wave amplitude and wave period but for detecting wave propagation direction at least two buoys are needed. Different sensors have been used on buoys for measuring such as down looking laser profiles, current meter triplets, pressure transducers.
However, when using buoys to measure the waves, these tend to drift with the water particle motion and give imprecise spatial measurement (see Fig.4 left side). In order to solve these problem different methods have been offered as an example see ref. [12]. In Fig. 4 right side a measurement buoy named WaveScan is depicted, this buoy measures heaven and sway acceleration [9].
1.3.2. Synthetic aperture radar
It has been amply demonstrated that synthetic aperture radar (SAR) data can be used to estimate parameters of the two-dimensional (2-D) sea surface elevation field [13, 14]. Due to their high spatial resolution and all-weather and daylight capabilities, spaceborne SAR systems are the only sensors that can provide directional ocean wave information on a continuous and global scale.
The SAR radar sends a pulse down to the ocean surface at nadir. The significant wave height is obtained from the slope of the leading edge of the return pulse, while the total backscatter gives us the wind speed. The major goals of the variable SARs were applications in ocean wave research and wave forecasting. Two-dimensional ocean wave spectra can be derived from SAR images by inversion of the SAR imaging mechanism.
Figure 4.
Left side; Error in measurement due to buoy movement. Right side; The WaveScan buoy [9].
2. Wave energy convertors
Ocean Waves has been considered as a source of energy since late 18th century and the first patent for capturing wave power was filled in France in 1799 by a father and son named Girard [15]. After World War I when petrol became most important source of energy the interest for harnessing ocean wave power faded. In 1940s, the Japanese wave power pioneer Yoshio Masuda developed an innovative device for absorbing wave power which is known as Oscillating Water Column (OWC) [16]. Oil crisis in 1973 was a great stimulator for governmental funds and researches in wave power extracting but petrol price decline in early 1980s abated interest in wave power [15]. Recently, the Kyoto Protocol on reduction of CO2emission, has intensified the interest in this field among researchers. To date, there are various devices which capture power from ocean waves [16, 17]. These devices are distinct in installation location (Off-shore, Near-shore and shoreline) as well as manner of energy harvesting. This section categorise Wave Energy Convertors (WECs) based on manner of interaction with ocean waves.
Excising WECs harvest wave power based on two different principles, Oscillating-WECs and Interface-WECs.
Oscillating-WECs are devices that are in direct contact with ocean waves and oscillate in specific direction related to device design and degree of freedom. J. Falnes, one of the distinguished pioneers in ocean wave power absorption, has been clarified that there are six degree of freedom for a body to oscillate with ocean waves [18]. According to Fig. 5, Oscillation in direction of 1st, 2ed and 3rd arrows are known as surge, sway and heave respectively. Also rotation around x-axis (mode 4), y-axis(mode 5) and z-axis (mode 6) are named respectively roll, pitch and yaw. Oscillating-WECs are displaced in only these six modes, most of these WECs have oscillation in only one of these modes which are known as single-mode oscillators and some others have oscillation in more than one mode that are regarded as multi-mode oscillators. (Note that in most of Oscillating-WECs there is no variation in y direction, in this case there are only three modes for body oscillation; Surge, Have and Pitch).
Figure 5.
Different oscillation mods of a Wave Energy Convertor: Surge (1), Sway (2), Heave (3), Roll (4), Pitch (5) and Yaw (6) [18].
Figure 6.
Categories of Wave Energy Convertors.
Interface-WECs are special forms of WECs that are not oscillating in aforementioned modes. In fact these WECs are devices or structures that are fixed in a location and have not interaction with ocean waves. Interface-WECs are used to deliver wave power by an interface (water or air) to the PTO (power take-off). The scheme of classification of WECs is illustrated in Fig. 6.
2.1. Oscillating-WECs
In this subsection, different WECs, which have one or two degrees of freedom, are investigated. Indeed, these WECs are simple in motion due to their restricted motion modes and they can be divided to three distinct categories; Heave Oscillators, Pitch Oscillators and Surge Oscillators.
2.1.1. Heaving oscillators
Heave Oscillators are the simplest oscillators for absorbing wave power. These devices, extract wave power with motion in perpendicular direction to the Sea Water Level and according to the mooring and working principle are divided to three groups; Buoys, Two Body Heaving Convertors and Submerged Heaving Convertors [16].
2.1.1.1. Buoy
Point absorbers or buoys are convertors with one floating body in sea level which is connected to the PTO (Power Take-Off) via a steel structure or a cable (translator). The body fluctuates with ocean waves in earth gravity direction (heave) which cause the steel structure or cable to oscillate with it hence the bidirectional movement of buoy is transferred to the PTO in the other point of translator and PTO generates electricity. To date various buoys have been designed for wave energy harvesting which are same in principal but different in detail. One of these is a buoy that was designed by Budal et al. in Norway [19]. The device was linked to anchor on the sea bed via universal joint (see Fig. 7). An air turbine was implemented on the device for energy converting and it was controlled by latching control.
Figure 7.
Norwegian buoy (courtesy of J. Falnes) [16].
Figure 8.
Left side; Taut moored heaving buoy with linear electrical machine PTO [16]. Right side; Component of tout moored WEC, Sweden [22].
Another buoy type is floating body connected to bottom fixed structure via a cable (taut moored). Due to cable flexibility, this device is not restricted in heave mode and it also has oscillation in surge direction. PTO of device is fixed in ocean bed and cable transfer WEC motion to PTO. There are two different PTO that has been coupled with this type of WEC. Hydraulic PTO was implemented by this WEC in Denmark in 1990s which by piston pump supplies high pressure water to a hydraulic turbine [20] and another is linear electric generator that is housed in inside a steel hull mounted on a concrete ballast structure and converts linear motion of cable (translator) to electric power [21]. This system is developed in Sweden and the scheme of system is represented in Fig.8. Barbarit et al. have investigated different power capture preformation of various WECs by numerical method [22] and capture width of taut-moored WEC is as Fig.9.
Figure 9.
Power capture performance of taut moored WEC for various waves (the vertical axis is wave amplitudes in meter and horizontal axis is wave period in second and the annual men absorbed power amount on the table are in kW) [22].
Figure 10.
Wave Star WEC, Denmark [22].
Figure 11.
Power capture performance of Wave Star WEC [22].
In the case of heaven buoys, Wave Star Energy company has developed an innovative WEC namely Wave Star WEC. In this device a jack up structure stands on sea bed and provides a reference to the buoys (see Fig. 10). A full sized system is consisting of different buoys in which a hinging arm is utilized to transfer each buoy’s motion to the PTO. The buoys have ability to be polled up (survival mode) in case harass ocean condition. Furthermore, hydraulic rams are employed to convert hinging motion of arms. Power capture preformation of 20 buoys Wave Star WEC was investigated by Babarit et el. [22] and the result is as Fig. 11.
2.1.1.2. Two body heaving convertors
Two body heaven convertors are multi-body convertors in which ocean power is extracted from the relevant motion between two bodies. One of these bodies is float on ocean surface and another is completely submerged. Ocean wave interaction with this WEC causes the float body elevates in heave mode as well as it pushes submerged body to the sea bottom due to increase in sea water inertia. One of the important advantages of this WEC is facility in its installation. Because device does not require any sea-bed connection, it can easily be installed in off-shore. Yet, different devices are developed in this principal one of which is ISP buoy developed in Sweden [23], Irish Wavebob [24] and PowerBuoy inspired by Ocean Power Technologies company.
The schematic of Wavebob is depicted in Fig. 12 left side. According this picture wavebob is consist of an inner buoy, submerged body (body2), and floating buoy (body 1) which are axially connected to each other. Additionally a high Pressure oil hydraulic system is implemented to deliver extracted power to electric generator. Fig. 13 illustrates power capture matrix of Wavebob WEC [22].
Figure 12.
Left side; Principle of Wavebob WEC [16]. Right side; ¼ Scale Wavebob WEC, Ireland [22].
The Archimedes Wave Swing (AWS) is a fully submerges off-shore WEC. It is constructed from two main parts, Silo or Basement is an air filled cylindrical chamber which is moored on seabed and floater is oscillating upper part as is illustrated in Fig. 14. Floater oscillates by water pressure variation. By crossing wave crest upon AWS the floater moves down compressing the air inside the chamber and by passage of wave trough upon AWS, the air inside the chamber expands and consequently push the floater up. Beside its unique design, AWS is the first WEC that a linear electric machine is implemented as PTO. One side of linear machine is fixed to the basement and the other side is connected to the floater via a translator, hence oscillation of floater excites linear machine. The AWS was successfully tested in 2004 [25].
Due to their mooring structure and the environment they work in (off-shore), almost all of the heaving oscillators requires highly maintenance. Meanwhile delivering generated electric power to the electric network or consumer is another problem intrinsically related to these off-shore WECs. High cost and Long distance underwater cabling is a commercial problem that heaving oscillators face with.
2.1.2. Pitching oscillators
Pitching oscillators are WECs which extract wave power by hinging motion in wave propagation direction. As it is demonstrated in Fig. 5, the hinging motion of pitching oscillator occurs in the axis in which WEC is installed on. According to device mooring and body design theses WECs are categorized to three types; Float Pitching Convertors, Two Body Pitching Convertors and Submerged Pitching Convertors.
2.1.2.1. Float pitching convertors
Developed in Lancaster University and off-shore WEC, PS Frog Mk 5 is the best example of Floating Pitching Convertors [26]. As it is illustrated in fig. 15, PS Frog Mk 5 is composed of a large buoyant paddle with an internal ballasted handle below it. It oscillates in pitching mode and is float on sea level. When wave acts on paddle the ballast provides necessary reaction for pitch motion, consequently the wave power is absorbed by partially resisting the sliding of a PTO mass, which moves in guides above sea level. The sliding mass (PTO) converts the wave motion into differential mechanical motion within device then the mechanical motion is transferred via hydraulic circuit to an electrical generator.
The main advantages of PS Frog Mk 5 is its self-orienting capability with which the device spontaneously adjusts to face incident waves. Meanwhile, by moving ballast in the hall or by controlling sliding mass, it is viable to control PS Frog Mk 5 in resonance frequency in which device has the maximum capture width.
Figure 15.
Left side: 2D illustration of PS Frog Mk 5 [16]. Right side: Perspective view of PS Frog Mk 5 [26].
2.1.2.2. Two body pitching convertors
Pelamis is a multi-body, floating, off-shore WEC. This device consists of several slender semi-submerged cylinders linked by hinged joins [27, 28]. When wave acts on Pelamis, adjacent cylinders start to fluctuating by angular motion in the joins in which wave power is absorbed in Pitch and Yaw mods. The scheme of Pelamis is presented in Fig. 16. In this figure, the left side represents the working concept of Pelamis and the right side shows a full scale Pelamis. In Pelamis the motion of cylinders is used to move hydraulic cylinders which pump fluid to high pressure fluid accumulators for short term energy storage. Furthermore, the smooth supply of high pressure fluid in accumulators drives hydraulic motors which are coupled with grid-connected electric generators. About device mooring, because of the self-referencing no rigid connection to the sea-bed is required and a slack mooring is sufficient to hold the device on station.
Figure 16.
Left side: Scheme of Pelamis and principle of working [27]. Right side: Full scale prototype (By Ocean Power Delivery Ltd).
The PTO section of Pelamis is divided to two main parts which are called primary and secondary transmissions. The primary transmission, which stores wave power in hydraulic accumulator, consists of the hydraulic cylinders and their controllers. The secondary transmission, consisting of hydraulic motors coupled to electric generators, converts the energy stored in the hydraulic accumulators into electricity transmitted to shore. The separation provided by high pressure accumulator and controlling of electronically controlled valves, which controls input and output fluid of accumulators, makes it feasible efficient power absorption from ocean waves.
Full scale prototype Pelamis WEC, 120 m long and 3.5 m diameter, has been constructed and has been successfully connected to local electrical power network.
2.1.2.3. Submerged pitching convertors
Yet, there are different devices that fall in this category [29, 30] one of which is Oyster [31], Aquamarine Power Ltd developed near-shore WEC. The Oyster is a bottom hinged rigid flap which completely penetrates the water column from above the surface to the sea bed. When wave attach the Oyster, WEC starts to oscillate in pitch mode, rotational motion around hinging axis, and this motion moves a double acting high pressure sea water pump. A set of non-return valves rectify the flow from the double acting pump consequently the flow is regulated by a gas accumulator. The flow (water) is transferred to the shore through pipeline. In the onshore hydraulic plant, hydraulic pressure is converted into electric power via a Pelton wheel. Finally the water passes back to device in a close lop via a second low pressure return pipeline. The schematic of Oyster is presented in fig. 17. Another WEC that work in the same principle is WaveRoller WEC. In spite of Oyster, the rigid flaps of WaveRoller are short and it harvests wave power only near seabed [30].
Figure 17.
Left Side: Schematic of pitching flap WEC. Right Side: The Oyster WEC by Aquamarine Power Ltd [32].
Figure 18.
The power matrix of bottom hinged pitching flap [22].
The power capture performance of submerged pitching convertor is presented in Fig. 18.
2.1.3. Surging oscillators
However, waves’ force in near-shores is concentrated in surge direction [8], surge wave energy convertors are less developed WECs in comparison to other types.
Developed in Western Ontario University namely “Surfing Wave Energy Convertor” is one of the surge WECs [33]. The Surfing Wave Energy Convertor is comprised of several paddles connected to a common drive train, which mechanically links them to an electric machine. The operating cycle begins with a paddle suspended in the path of the incoming wave. As the waves impact the paddle it is driven horizontally in the direction of wave travel in a ‘Surfing’ like motion. The horizontal motion of the paddle in-turn drives the electric machine, generating power. Once the paddle reaches the downstream end of the system, the electric machine is switched to motor operation and drives the system, lifting the first paddle out of the path of the waves and lowering the next paddle into the wave path.
Figure 19.
Schematic of Surge WEC.
Another surge WEC is designed by these authors [34, 35]. It consists of a rigid plate which is installed in near-shore vertical to the sea bed. The plate has been connected to a linear generator. When waves attack the plate it fluctuate in horizontal direction, parallel to the wave propagation direction (See Fig. 19). Various power electronic instruments has been implemented to deliver ocean wave power to electric network. The device is still under development in Altin Tara Electric Ltd. in Iran.
2.2. Interface-WECs
Interface-WECs are device that have no oscillation in interacting ocean wave. In fact these devices are designed to deliver wave energy via an interface (Air or Water) to the PTO. In comparison to Oscillation-WECs they require less maintain.
2.2.1. Air-interface
Oscillating water column (OWC) WEC is an Air-interface WEC in which wave power is converted to the electrical power without direct oscillation of WEC body by water particle. OWC is consists of a floating or bottom fixed structure whose upper part encloses a column of air and whose immersed part is open to the wave action [36]. The scheme of OWC is presented in Fig. 20.
When waves attack the OWC, the water pressure below the chamber compresses the trapped air in the chamber and the air is guided to a turbine hence the flow of air to outside of chamber turns the turbine and the coupled generator. Meanwhile, by decline of water pressure below the chamber, the pressure of trapped air reduces and consequently air flows into chamber and drives the turbine again. To date, two type of self-rectifying turbine has been used in OWC; the Well Turbine and Impulse Turbine, both of which have the capacity to rectify air flow that makes it feasible to have unidirectional motion in electrical generator.
The early inventor and developer of OWC is Yoshio Masuda who had commercialized the floating OWC in Japan since 1965 [16]. The OWC has been used for energy converting in both shoreline and near-shore.
Figure 20.
Left side: Schematic of OWC. Right side: Back view of an OWC [37].
2.2.2. Water-interface
Overtopping wave energy convertors are the main members of water-interface WEC. To date, three overtopping wave energy convertor has been developed; The Tapchan (Tapered Channel Wave Power Device) [38], Wave Dragon [39] and SSG (Seawave Slot-Cone Generator) [40]. One of the well-known overtopping WECs is Wave Dragon. The Wave Dragon is an off-shore WEC, installed in location with depth of 25-40m, which is moored like a ship and consists of three main sections. The main platform, a reservoir with a double curved ramp, is float on the ocean surface and other parts are mounted on it. Two wave reflectors are installed on both sides of platform and intensify wave amplitude approaching to the platform. Finally a Hydro turbine, a set of low head Kaplan turbine, converts the hydraulic head in the reservoir. The Wave Dragon is represented in Fig. 21.
When waves approach to Wave Dragon, the reflectors focus them and guide the water toward the ramp, water overtop the ramp and fill in the reservoir then the turbine generates electricity from water motion inside the device. In Wave Dragon the wave energy convertor has not oscillation with wave, indeed wave power is transferred to PTO by water. In spite of air-interface WECs, water-interface WECs are not capable to be analyzed by Linearized Wave Theories.
In process of wave energy convertion, after power extraction in WEC, another energy conversion happens in Power Take-Off (PTO). Power take-Off is (mostly mechanical or hydraulic) device in which the absorbed power is transferred to an electric generator. To date, three type of PTO is more commonly used.
Air/Water Turbine forms part of an integral system that consists of a capture device, which also includes an electric generator. This PTO system is used in Interface-WECs (Oscillating wave columns and Overtopping devices). The air turbines which are used in OWC are mostly self-rectifying turbines which convert reciprocating air flow to unidirectional torque. The two implemented turbine in OWC are Well turbine [41] and Impulse turbine [42]. Probably one of the advantages of turbines in PTO is facility of using flywheel for energy storage.
Hydraulics PTO system is consisting of a hydraulic circuit which transfers absorbed power of wave to a hydraulic motor which drives an electrical generator [43]. This kind of PTO is used in Pelamis and bottom hinged pitching flap. Implementation of accumulator is an effective method for energy storing in this PTO.
Direct Drive is consisting of a moving part named translator on which linear generators is mounted. Direct drive is the simplest and probably the most efficient Power Take-Off system. PTO system of heaving oscillators and submerge heaving oscillators are from this kind.
Regard less to the type of PTO, all of the PTOs are connected to an electrical generator which generates useful energy from waves (except especial uses of WEC that is not intended to generate electricity [32]). The two type of electrical generators implemented in WECs are Linear Generators and Rotational Generator.
3.1. Linear generators
Linear generator are the kind of electrical machine in which the rotor (translator) and stator are linear and translator displace in straight path inside stator. Since most of the WECs harness wave power in reciprocating directions, Linear Generators are the most appropriate machines for generating electricity by WECs. It is due to, there is not require for any other interface or other power conversion (e.g. Hydraulic) which decline the transferred power in transmission process. Linear generator is connected to the WEC via translator and displace with it. Yet, three topology of linear generators are considered in wave energy industry.
3.1.1. Linear Permanent Magnet Synchronous Machine (LPMSM)
LPMSAs are constructed in three different configuration; Single-Side, Double–Side and Tubular. In all of these structures the translator (actuator) have moving magnets and primary constitute mover. The core of the primary of a flat LPMSA is made of longitudinal laminations with uniformly distributed slots, which house the windings. Since the windings are located in open slots, the effective air gap is greater than the actual air gap.
In tubular structures the laminations of the shape primary core is longitudinal or disk-shaped. Stacking of the disk laminations increases the effective air gap. The core of the secondary of a tubular LPMSA is generally made of solid magnetic steel. In LPMSM the flux density is supplied by rare earth permanent magnet. Due to ease in assembly, disk shaped laminated tubular LPMSM are preferred to flat types also slitting technique is use on disk lamination to reduce eddy current [44]. The schematic of single side LPMSM is illustrated in Fig. 22.
A family of permanent magnet machine, known as variable reluctance permanent magnet machine (VRM), has been developed with high force density. Despite its high force density, low power factor is a characteristic of VRM machines. The machine has a very high inductance, such that the current can be out of phase for almost 90 degree. The variable reluctance permanent magnet family is divided for two subcategory; Transverse Flux Permanent Magnet (TFM) and Vernier Hybrid Machine (VHM).
Transverse Flux Permanent Magnet Machines (TFM) has higher shear stresses than other machine topologies, This implies that TFM machines may be more suitable for wave energy application than the synchronous machines. There are two topology of TFM. In the first topology, the coils are in the stator and the magnets are on the translator. The translator is longer than the stator, which means that a part of the (rather expensive) magnets is not used (see Fig. 22. Left). This machine was used in AWS.
Figure 23.
Left side: TFM machine with flux concentration and moving magnets [45]. Right side: TFM machine with flux concentration and stationary magnets [45].
As it is illustrated in Fig. 22 Right, the second topology, namely the double-sided moving-iron TFM, is a double-sided machine in which the translator consists only of iron. “In this topology, the stator consists of coils and U-cores on both sides of the translator, which consists of two rows of magnets and flux concentrators with space for construction material in between. Both the conductors and the magnets are kept stationary. The U-cores are now simpler in shape because space for coils is no longer required, and these cores or yokes form the translator.”[45]
3.1.2.2. Vernier Hybrid Machine (VHM)
The Vernier Hybrid Machine is constructed from a linear toothed translator constructed from iron laminates which move inside two C-cores. The C-core has coil wounded on each pole also magnets are mounted on pole face. The translator tooth and slots width are similar in dimension to the magnet pitch, hence rapid flus reversal happens over short distance as the translator teeth move from the aligned to the unaligned position. Due to rapid flow change in a short distance, the electric frequency of the flux pulsation is greater than the translator’s frequency [46, 47]. The schematic of one pole VHM is presented in Fig. 24. In spite of TFM, the VHM can be constructed from lamination which makes construction easy and small. However power factor of VHM is low, the high shear stress, small sizes and facility of constructing are main advantages of this machine.
3.1.3. Tubular air cored permanent magnet generator (TAPM)
The TAPM machine is proposed for wave application by Baker and Muller [48]. The principle of TAPM is shown in Fig. 25. In this topology, the magnets are magnetized in the axial directions with altering direction of flux [37]. Flux concentrators are placed between the magnets and a varying flux wave is created outside the translator. The large constructional advantage of TAPM is elimination of normal force by removing the steel in stator. Significant support structures are needed to overcome these forces and maintain a constant air gap width. The main problem in this topology is that the magnetic reluctance in the magnetic circuit is increased considerably, since the distance the flux travels in air now is in the range of the pole pitch and not, as in steel stator machines, just over the air gap [37]. The flux of an air cored machine is thus much smaller and the power per air gap area is considerably lower.
Figure 24.
One phase of Linear Vernier Hybrid Machine [46].
Figure 25.
Tubular Air Cored Permanent Magnet Machine [37]. (Left side: Three dimensional view. Right Side: Cross section view)
Figure 26.
Common used power electronic circuit for connecting linear generator to the electrical network.
Regardless to the type of the linear machine, a linear machine generates fluctuating voltage from reciprocating motion of WEC, which is varying in both amplitude and frequency. Thus, it is not possible to connect linear generator directly to electric grid. For solving this problem, effective power electronic instrument is implemented [49]. One of the common power electronic circuits, implemented with linear generator, has a diode bridge rectifier or invertor rectifier in generator side, in which the generated voltage is delivered to a battery or capacitor after rectifying. Also another invertor is used in grid side to deliver power in DC-Link (battery or capacitor) to the electric. This power electronic circuit is depicted in Fig. 26.
3.2. Rotational generators
However utilization of rotational generator in wave industry is a questionable issue, conventional generators have been used with different wave energy convertors. Pelamis, Oscillating Water Column and overtopping devices are the main WECs which use rotational generator for mechanical electrical conversion. In these cases, the Asynchronous Generator or Induction machine is a preferred machine. It is due to the capacity of this type of machine to act in variable speed condition. Meanwhile, utilization of wound rotor induction machine makes it feasible to control rotor current and frequency which in consequence control the velocity and extracted power by mechanical part (This use of induction machine is so called Double Fed Induction Generator (DFIG)). Amundarain et al. considered the DFIG on OWC for controlling the electrical machine in a proper manner [50]. In comparison to the linear machine, it is much more simple to connect an induction machine to the electrical grid. While, since these machines was designed to act in higher speed, in most of the cases the utilization of rotational machine for convert low speed WEC motion is a low effective manner.
4. Environmental consequences
Renewable sources have been considered as new source of energy to decline our dependence on fossil fuel and be a solution to the global warming and CO2 emission. Considering, each technology (WEC) beside its advantage might have some side effect and by taking into account the importance of environment in which a wave energy convertor acts (Ocean), finding out and preventing possible negative consequence of WEC carries a huge importance. Thus, before any decision to build a large WEC farm this issue should be considered accurately to prevent occurring of any other disaster like CO2 emission and global warming. There are some probable problems that may afflict the ecosystem as a consequence of WEC application, some of which is as follow;
Constructing Wave Farm in a location might cause military importance of location, avoidance of shipping and fishing which not only might change the economy of area but also cause a biological change in the area [51]. The WECs are attractive to the fish and it is due to fish use these devices as protection from predator, availability of food near them, spewing substrates and so on [52]. Hence, restriction for fishing and popularity of WECs by fish may enhance fish population in Wave Farm and this has a negative impact on local species diversity and population density [53].
WECs alter the currents and waves in implemented area and this might change sediment size distribution in area which may favour the accumulation of organic material in area [54].
It was indicated that some species of shark are sensitive to the electromagnetic field of 25-100 uT [55] and also it was shown that migrating European eels can detect the magnetic field of underwater cables [56]. It is worthwhile to find out possible consequence of external electromagnetic field on marine species and reduce the emitted magnetic field from under water cables.
Noises generation during site construction, maintenance and even normal working of WEC can affect dolphin, whales, seals and other fish species, which use underwater sound for communication and finding mat and so on [57, 58]. However little is known about long-term effects of noise on these species, the possible preventing technics should be developed for less interacting of WECs in ocean environment.
5. Conclusion
This chapter presents essential information about generation and potential of ocean wave power. Also the available Wave Energy Convertors has been categorized according to the principle of interaction with ocean waves. The manners of acting and mooring and in some case the average power output of WECs are presented. Meanwhile, the implemented electrical generator by WECs has been described in section three. Finally the possible environmental consequence of WECs has been investigated at the end of this chapter. This chapter reviews the available technologies of harnessing wave power.
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Surging oscillators",level:"3"},{id:"sec_17_2",title:"2.2. Interface-WECs",level:"2"},{id:"sec_17_3",title:"2.2.1. Air-interface",level:"3"},{id:"sec_18_3",title:"2.2.2. Water-interface",level:"3"},{id:"sec_21",title:"3. Power take-off",level:"1"},{id:"sec_21_2",title:"3.1. Linear generators",level:"2"},{id:"sec_21_3",title:"3.1.1. Linear Permanent Magnet Synchronous Machine (LPMSM)",level:"3"},{id:"sec_22_3",title:"3.1.2. Variable Reluctance Permanent Magnet Machine (VRM)",level:"3"},{id:"sec_22_4",title:"3.1.2.1. Transverse Flux Permanent Magnet Machine (TFM)",level:"4"},{id:"sec_23_4",title:"3.1.2.2. Vernier Hybrid Machine (VHM)",level:"4"},{id:"sec_25_3",title:"3.1.3. Tubular air cored permanent magnet generator (TAPM)",level:"3"},{id:"sec_27_2",title:"3.2. Rotational generators",level:"2"},{id:"sec_29",title:"4. Environmental consequences ",level:"1"},{id:"sec_30",title:"5. Conclusion",level:"1"}],chapterReferences:[{id:"B1",body:'A. H. Strahler and A. N. Strahler. 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Henry. 34, 2007, Ocean Engineering, pp. 1265–1274.'},{id:"B9",body:'Stephen Barstow, Gunnar Mørk, Denis Mollison and João Cruz. The Wave Energy Resource. [book auth.] João Cruz. OceanWave Energy Current Status and Future Prepectives. Berlin : Springer-Verlag, 2008.'},{id:"B10",body:'The Norwegian ‘‘wave climate mapping’’ programme. Torsethaugen, K. Tapir, Trondheim, Norway : s.n., 1982. Proceedings of the second international symposium on wave energy utilization. pp. 81–97.'},{id:"B11",body:'Wave prediction based on a modified grey model MGM(1,1) for real-time control of wave energy converters in irregular waves. D.Q. Truong, K.K. Ahn. 2012, Renewable Energy.'},{id:"B12",body:'An application of the Fast Fourier Transform to the short-term prediction of sea wave behaviour. J. Ross Halliday a, David G. Dorrell, Alan R. Wood. 36, 2011, Renewable Energy, p. 685e1692.'},{id:"B13",body:'Measurement of 2-D Sea Surface Elevation Fields Using Complex Synthetic Aperture Radar Data. Johannes Schulz-Stellenfleth and Susanne Lehner. 6, 2004, IEEE Transactions on Geoscience and Remote Sensing, Vol. 42, pp. 1149-1160.'},{id:"B14",body:'Ocean wave extraction from RADARSAT synthetic aperture radar inter-look image cross spectra,. M. Dowd and P.W. Vachon. 2001, IEEE Transactions on Geoscience and Remote Sensing, Vol. 39, pp. 21-37.'},{id:"B15",body:'Ross, D. Power from sea waves. Oxford : Oxford University Press, 1995.'},{id:"B16",body:'Wave energy utilization: A review of the technologies. Falcao, Antonio F. de O. 3, 2010, Renewable and Sustainable Energy Reviews, Vol. 14, pp. 899–918.'},{id:"B17",body:'A review of wave-energy extraction. Falnes, Johannes. 4, 2007, Marine Structures, Vol. 20, pp. 185-201.'},{id:"B18",body:'Falnes, Johannes. Ocean Waves and Oscillating systems. Cambridge : Cambridge University Press, 2004.'},{id:"B19",body:'The Norwegian wave-power buoy project. Budal K, Falnes J, Iversen LC, Lillebekken PM, Oltedal G, Hals, et al. Trondheim, Norway : Proceedings of 2nd International Symposium on Wave Energy Utilization, 1982. pp. 323–44.'},{id:"B20",body:'Point absorber—optimization and survival testing. Nielsen K, Smed PF,. s.l. : Proceedings of 3rd European Wave Energy Conference, 1998. 207–14.'},{id:"B21",body:'Experimental results from sea trials of an offshore wave energy system. Waters R, Stalberg M, Danielsson O, Svensson O, Gustafsson S, Stromstedt E, et al. 90, s.l. : Applied Physics Letters, 2007, Vol. 3.'},{id:"B22",body:'Numerical benchmarking study of a selection of wave energy converters. A. Babarit, J. Hals, M.J. Muliawan, A. Kurniawan, T. Moan, J. Krokstad. s.l. : Renewable Energy, 2012, Vol. 41, pp. 44-63.'},{id:"B23",body:'Contribution to the theory andexperience of energy production and transmission from the buoy-concept. Cleason L, Forsberg J, Rylander A, Sjostro mBO,. s.l. : Proceedings of 2nd International Symposium on Wave Energy Utilization, 1982. pp. 345–70.'},{id:"B24",body:'Wavebob—research & development network and tools in the context of systems engineering. Weber J, Mouwen F, Parrish A, Robertson D. s.l. : Proceedings of 8th European Wave Tidal Energy Conference, 2009. pp. 416–20.'},{id:"B25",body:'Learning experience of AWS pilot plant test offshore Portugal. FE, Gardner. s.l. : Proceedings of 6th European Wave Energy Conference, 2005. pp. 149–54.'},{id:"B26",body:'Developments in the design of the PS Frog Mk 5 wave energy converter. McCabe AP, Bradshaw A, Meadowcroft JAC, Aggidis G. 2006, Renewable Energy, Vol. 31, pp. 141-51.'},{id:"B27",body:'Design, simulation, and testing of a novel hydraulic power take-off system for the Pelamis wave energy converter. Henderson, Ross. 2006, Renewable Energy, Vol. 31, pp. 271–283.'},{id:"B28",body:'Measurements of the slow drift dynamics of a model Pelamis wave energy converter. Retzler, Chris. 2006, Renewable Energy, Vol. 31, pp. 257–269.'},{id:"B29",body:'WaveNet. European Community. 2003. ERK5-CT-1999-20001.'},{id:"B30",body:'Company, AW-Energy. http://www.aw-energy.com/concept.html. [Online] AW-Energy Company. '},{id:"B31",body:'Design of the Next Generation of the Oyster Wave Energy Converter. L. Cameron, R. Doherty, A. Henry, K. Doherty, J. Van ’t Hoff, D. Kaye and D. Naylor, S. Bourdier, T. Whittaker. Bilbao : s.n., 2010 October. 3rd International Conference on Ocean Energy.'},{id:"B32",body:'The cost of water from an autonomous wave-powered desalination plant. Matt Folley, Trevor Whittaker. 2009, Renewable Energy, Vol. 34, pp. 75–81.'},{id:"B33",body:'Electric power generation by ‘Surfing’ water waves. Ben D. Hazlett, Ion I. Inculet a, Diana R. Inculet. 2009, Renewable Energy, Vol. 34, pp. 2510–2514.'},{id:"B34",body:'Enferad, Ehsan. Engine for Producing Energy from Sea Waves. 47700 Iran, April 2008.'},{id:"B35",body:'Application of PMSM for Electric Generation from Ocean Waves by EPEW. Ehsan Enferad, Murtaza Farsadi and Shirin Enferad. Bursa, Turkey : s.n., 2011. nternational Conference of ELECO. pp. 258-262.'},{id:"B36",body:'OWC wave energy devices with air flow control. A.F. de O. Falcao, P.A.P. Justinob. 1999, Ocean Engineering, Vol. 26, pp. 1275–1295.'},{id:"B37",body:'Cruz, João. Ocean Wave Energy Current Status and Future Prepectives. Berlin : Springer-Verlag, 2008.'},{id:"B38",body:'Evans DV, Falcao A.F. de O. Mehlum E Tapchan. Hydrodynamics of ocean wave energy utilization. Berlin : Springer, 1989.'},{id:"B39",body:'Prototype testing of the wave energy converter Wave Dragon. Kofoed JP, Frigaard P, Friis-Madsen E, Sørensen HC. 2006, Renewable Energy, Vol. 31, pp. 181-189.'},{id:"B40",body:'SSG wave energy converter: Design, reliability and hydraulic performance of an innovative overtopping device. L. Margheritini, D. Vicinanza b, P. Frigaard. 2009, Renewable Energy, Vol. 34, pp. 1371-1380.'},{id:"B41",body:'AA, Wells. Fluid driven rotary transducer. Spec No. 1595700 British Patent, 1976.'},{id:"B42",body:'IA, Babinsten. Apparatus for converting sea wave energy into electrical energy. No. 3922739 U.S. patent, 1975.'},{id:"B43",body:'Power conversion mechanisms for wave energy. Salter SH, Taylor JRM, Caldwell NJ. 2002, Proc Inst Mech Eng Part M J Eng Maritime Environ, Vol. 216, pp. 1-27.'},{id:"B44",body:'I. Boldea, Syed A. Nasar. Linear Electric Actuators and Generators. s.l. : Cambridge University Press, 1997.'},{id:"B45",body:'Conventional and TFPM Linear Generators for Direct-Drive Wave Energy Conversion. Henk Polinder, Barrie C. Mecrow, Alan G. Jack, Phillip G. Dickinson, and Markus A. Mueller. 2, 2005, IEEE TRANSACTIONS ON ENERGY CONVERSION, Vol. 20.'},{id:"B46",body:'Power conditioning of the output from a linear vernier hybrid permanent magnet generator for use in direct drive wave energy converters. P.R.M. Brooking and M.A. Mueller. 2, 2005, IEE Proc.-Gener. Transm. Distrib, Vol. 152.'},{id:"B47",body:'Modelling the performance of the vernier hybrid machine. M.A. Mueller and N.J. Baker. 6, 2003, IEE Proc.-Electr. Power Appl, Vol. 150.'},{id:"B48",body:'Permanent magnet air-cored tubular linear generator for marine energy converters. Baker NJ, Mueller MA. Edinburgh : s.n., 2004. IEE Power Electronics and Electrical Machines & Drives Conference.'},{id:"B49",body:'Experimental verification of linear generator control for direct drive wave energy conversion. J.K.H. Shek D.E. Macpherson M.A. Mueller. 5, IET Renewable Power Generation, Vol. 4, pp. 395–403.'},{id:"B50",body:'Wave energy plants: Control strategies for avoiding the stalling behaviour in the Wells turbine. Modesto Amundarain, Mikel Alberdi, Aitor J. Garrido, Izaskun Garrido, Javier Maseda. 2010, Renewable Energy, Vol. 35, pp. 2639-2648.'},{id:"B51",body:'The impact of marine reserves: do reserves work and does reserve size matter? BS, Halpern. 2003, Ecological Applications, Vol. 13.'},{id:"B52",body:'Urban structures as marine habitats: an experimental comparison of the composition and abundance of subtidal epibiota among pilings, pontoons and rocky reefs. SD, Connell. 2001, Marine Environmental Research, Vol. 53, pp. 115–125.'},{id:"B53",body:'Temporal changes in the composition and abundance of the macro-benthic invertebrate communities at dredged material disposal sites in the Anse a Beaufils, baie des Chaleurs, eastern Canada. Harvey M, Gauthier D, Munro J. 1998, Marine Pollution Bulletin, Vol. 36, pp. 41–55.'},{id:"B54",body:'Effects of an artificial reef on the surrounding soft-bottom community (central Adriatic Sea). Fabi G, Luccarini F, Panfili M, Solustri C, Spagnolo A. 2002, ICES Journal of Marine Science, Vol. 59, pp. 343–349.'},{id:"B55",body:'Sharks can detect changes in the geomagnetic field. Meyer CG, Holland KN, Papastamatiou YP. 2004, J R Soc Interface, Vol. 2, pp. 129–30.'},{id:"B56",body:'Orientation of silver eel (Anguilla anguilla) in a disturbed geomagnetic field. Westerberg H, Begout-Anras ML. 2000. Proceedings of the 3rd Conference on Fish Telemetry. pp. 149–58.'},{id:"B57",body:'Sound detection and processing by fish: critical review and major research questions. Popper AN, Fay RR. 1993, Brain Behavior and Evolution, Vol. 41, pp. 14–38.'},{id:"B58",body:'Attraction of settlementstage coral reef fishes to reef noise. Simpson SD, Meekan MG, McCauley RD, Jeffs A. 2004, Marine Ecology Progress Series, Vol. 276, pp. 263–8.'}],footnotes:[],contributors:[{corresp:"yes",contributorFullName:"Ehsan Enferad",address:"st_e.enferad@urmia.ac.ir",affiliation:'
Altin Tara Electric Ltd, Urmia, Iran
Department of Electrical Engineering, Urmia University, Urmia, Iran
Department of Electrical Engineering, Urmia University, Urmia, Iran
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1. Introduction
Ciliates (Alveolata: Ciliophora) comprise free-living and symbiotic species. According to Corliss, [1] 2,600 species of ciliates have been described as symbionts, mainly of individuals of metazoan phyla. This is equivalent to 33% of all the known species of the phylum. They belong to eight classes (Armophorea, Heterotrichea, Litostomatea, Nassophorea, Oligohymenophorea, Plagiopylea, Phyllopharyngea and Spirotrichea), 31 orders, 151 families, and almost 700 genera [2]. These symbiotic ciliates have been reported in aerobic and anaerobic environments and from aquatic and terrestrial habitats [2, 3].
The term symbiosis can be defined as a sustained relationship between at least two individuals from different species, either living in direct contact or close enough to each other during a part or the whole life cycles of the partners. This interaction is transmitted vertically (from one generation to the next) or horizontally (acquired de novo in each generation). The intricate associations are believed to have an essential driving force in evolutionary biology, as a host and their symbiotic microbiota acclimatize on scales of short time [4].
Due to the diversity of symbioses, a classification system for symbiotic associations has been developed. This classification is based on several features: i) the dependence, where symbionts can be obligate or facultative; ii) specificity of the symbionts; iii) nutrients obtention, then biotrophic and necrotrophic symbionts are distinguished on the basis of whether nutrients are obtained from a living or dead partner, and iv) location of the symbionts, ectosymbionts or endosymbionts [5]. The symbiotic relationships can be categorized into mutualistic, commensalistic, or parasitic [2, 6]. The boundary between these categories sometimes is not clear, and there are frequent transitions between them.
Several papers have been focused on providing taxonomic reports for symbiotic ciliates, some of them as general works, and a few directed to certain groups [7, 8, 9, 10, 11, 12, 13, 14, 15, 16], and some were focused on certain geographic areas [17, 18, 19, 20, 21, 22, 23, 24]. Critical reviews of some species as Balantidium coli were done by Schuster and Ramirez-Avila [25]; for chonotrichs [26]; peritrichs [27] and suctorians [28].
Also, very different topics about ciliates and their hosts have been developed as shown: symbiotic interactions [epibiotic, hyperepibiotic, commensals, parasites (obligates and facultatives)], codiversification: [29, 30, 31, 32, 33, 34, 35, 36, 37]. Morphology (variation, molecular characterization): [38], clevellandellid, Nyctotheroides; [39], Dicontophrya; [40, 41] peritrichs. Taxonomy (new family, genus or species), redescription, revision: Apostomatia: [42]; Apostomatida: [43]; Trichodina: [44]; Epistylis and Opercularia: [45]; Spirochona: [46]; Buetschlia and Charonina: [31, 47, 48, 49, 50, 51]. Life cycles, encystment/excystment process: [52, 53, 54]. Pathogenicity, damages, infestation degree, virulence: [55, 56, 57, 58, 59]. Molecular and phylogeny: [30, 60, 61, 62, 63, 64, 65, 66, 67, 68]. Ecological aspects: [69, 70]. Immunity: [71, 72]. Stomatogenesis: [73]. Ultrastructure: [74].
Symbiotic systems between ciliates/animals are present in a broad spectrum of kingdom Animalia, and some examples are the following (animal group alphabetically arranged, different taxonomic levels): acari: [75]; amphipods: [76]; antilope: [77]; anuran: [78]; Asian elephant: [79]; baboon: [80]; bryozoans: [81]; buffaloes: [82]; capybara: [83, 84, 85]; cattle: [86]; chimpanzees: [87]; cirripedians: [88]; crustaceans: [89]; ctenophores: [90]; cuttlefish: [91]; dromedary camels: [92]; elephants: [93]; fishes: [94, 95]; frogs: [96]; great apes: [97]; horses: [98, 99]; humans: [100, 101]; polyps of hydras: [102]; insects: [103]; isopods: [104, 105]; kinorhynchs: [106]; llamas: [107]; maccacus: [108]; mammals: [109]; mollusks: [71, 76]; nematodes: [29, 110]; nemerteans: [13]; oligochaetes: [111, 112]; ostracods: [113]; polychaetes: [114, 115]; rhinoceroses: [116]; sea urchins: [117]; thoroughbreds: [118]; turbellarians: [119]; wood-feeding roaches: [120].
Some examples of ciliate taxa that include symbiotic species are the following:
Heterotrichea: Folliculinids attach to the integument of various invertebrates as bivalve shells, crustaceans exoskeleton, polychaete tubes, hydroid perisarcs, bryozoan tests, with a widespread occurrence [121], and may cause the skeletal eroding band or brown band diseases of scleractinian corals [2]; their life cycle includes a migratory swimming stage.
Spirotrichea: Hypotrichs are known mainly as free-living organisms, but some species such as Euplotes balteatus have been recorded in some sea urchins’ intestinal tract [122]. Some species of stichotrichids as Plagiotoma lumbrici are endosymbionts of oligochaetes [123].
Armophorea: Class Armophorea includes clevellandellids as Nyctotheridae, with obligate endosymbionts usually as commensals of invertebrates and vertebrates; life cycles include a phase of the cyst [2].
Litostomatea: Trichostomes are symbionts of vertebrates as ruminants and foregut fermenters [2], including the human pathogen, Balantidium coli, species that have a life cycle including two phases: trophozoites and cysts [25]. This species has been considered to be included in a new genus, Neobalantidium coli [124]. The genus Balantidium has a more significant number of species that have been reported as endocommensals in the digestive tracts of a widely diverse range of metazoan, as mollusks, arthropods, fishes, reptiles, birds, and mammals [124]. In the rumen ecosystem, ciliates can account for up to 50% of the total microbial nitrogen, reaching densities of 105 to 106 cells/ml rumen fluid, being Charonina ventriculi one of the smallest rumen ciliates [125].
Ophryoscolecidae and Cycloposthiidae include species as endosymbionts of ruminants and equids, respectively [126]. Entodiniomorphid ciliates of the genus Triplumaria are found in the intestine of elephants and rhinoceroses [60]. Entodiniomorphida do not form cysts, and in non-ruminant mammals, the infections of hosts occur by coprophagy [47].
Phyllopharyngea: Chonotrichs live on marine and freshwater hosts and divide by forming external or internal buds [127], with a dimorphism where the adults live attached to several appendages of crustaceans, and the larva is free and swims to reach a new host [128].
Suctorians, as a rule, reproduce by different modes of budding, produce one to several larvae, with a short swimming existence, and then lose their cilia and metamorphose into adults or trophonts [127]. The non-ciliated mature stages of suctorians are usually sessile, attached to the substrate by a non-contractile stalk, and reproduce by ciliary larvae called swarmers or migrators [129].
Oligohymenophorea: Yi et al. [130] documented that the life cycle of Ichthyophthirius multifiliis, a parasite of fish, consists of three key developmental stages: the infective theront, the parasitic trophont, and the reproductive tomont.
Mesanophrys pugettensis, is a scuticociliate thata was observed with a diphasic life history, the larger phase or trophont, and the smaller phase resembling tomites [34], is a facultative parasite of the Dungeness crab. Conchophthirus species are generally considered an endocommensal inhabiting the mantle cavity of freshwater clams or mussels [30].
Thigmotrichids from several families were analyzed by Raabe [131, 132, 133, 134], where species of Hemispeiridae are symbionts of the mantle cavity and nephridia of molluscan, those of Ancistrocomidae, Sphenopryidae and Thigmophryidae are ectosymbionts of mantle cavity and gills of molluscan, and Hysterocinetidae species were categorized as endoparasites of the gut of prosobranch mollusks; life cycles include tomites.
The apostomes is a small group of oligohymenophorean ciliates, with four major life histories: 1-exuviotrophic, that remain encysted on the exoskeleton of a crustacean host, and excyst to feed on exuvial fluid, reproducing during the host ecdysis, 2-sanguicolous, penetrate the cuticle of the host, feed on the cells and fluid of the hemocoel and reproduces, 3-chromidinid, found in the renal organs and opalinopsids found in the liver and intestines of cephalopods ingesting fluids and cells, 4-histotrophs, such as Vampyrophrya [135]. Apostome ciliates have life cycles typically involving crustaceans, with a non feeding microstome tomite and a macrostomous trophont [127]. Species of apostome of genus Collinia are endoparasites able to reproduce rapidly within the host that invariably kill the euphausiid within 40 hours of infection; Gymnodinioides genus includes exuviotrophic species that feed on the fluid within the exuviae of crustacean hosts and Landers et al., [136] documented for Gymnodinioides pacifica the presence of trophonts, phoronts, tomonts and tomites. For Synophrya the phoront, hypertrophont, hypertomont, and hypertomites were observed [137].
Pilisuctorian ciliates spend most of their lives perched on cuticular setae of crustaceans, and complete their life cycle on a single host, having the stages tomite, tomont and trophont [138].
In peritrichs, a significant character is the scopula which is the region that originates the stalk to attach the organism to the substrate and modifies to a highly complicated adhesive apparatus in mobiline [127]; two phases are known, the trophont and the dispersive telotroch.
Species of sessile peritrichs genera such Ambiphrya, Epistylis, Heteropolaria, Rhabdostyla, and Zoothamnium are epibionts of zooplanktonic invertebrates, larval stages of aquatic insects, aquatic mollusks, crustaceans, fish, amphibians, and reptiles as the main groups of organisms [139]. Members of genus Epistylis have been reported as epibionts in several metazoans, but also as an important fish ectoparasite being considered an emerging pathogen [140]. Genus Lagenophrys comprises only symbiotic species of freshwater and marine crustaceans [89]. Trichodinids are the most devastating ectoparasites of cultured fish, causing severe damage [141], and for genus Trichodina about 300 species have been described, mostly from freshwater environments [142]. Also, there are reports of trichodinids from the gills of limpets [143] and have been documented as symbionts of a broad spectrum of aquatic and terrestrial invertebrates and vertebrates hosts [65]. Trichodinella epizootica is one of the most widely distributed freshwater trichodinids in Europe and Asia, but has also been reported from Africa, the Pacific region and North America [55]. Urceolaria includes species ectosymbionts of freshwater turbellarians, marine polychaetes, and mollusks; Leiotrocha species are ectocommensals and endocommensals of marine molluscans, and species of Polycycla are endocommensals of Holothuroidea [144].
2. Ecological relationships: Classical definitions and approaches
2.1 Epibiosis
Epibiosis is a facultative association of two organisms: the epibiont, which colonizes the surface of live substrates, and the basibiont, which hosts the epibionts [145]. Some species of epibiotic communities show preferences for specific location sites on the host [76]. According to Wahl and Mark [146], when the effects associated with epibiosis are neutral or positive for a basibiont species and beneficial for an epibiont species, selection should favor the evolution of the epibiotic relationship, which tends to increase specificity through evolutionary history. Although many epibiont ciliates are not harmful to their basibionts, some studies have shown that the epibionts can cause deleterious effects on their hosts [147, 148, 149].
Historically, studies involving epibiont ciliates focus on the following interests: new records and checklists [27, 28], descriptions of new taxa using morphological and molecular data [150], possible deleterious effects on hosts [149, 151], distribution and preferred sites of epibiont populations and communities [152], spatial and temporal distribution of the epibiotic relationship [153], laboratory rearing and experimentation studies [154, 155, 156], and even investigations into extrinsic and intrinsic factors involved in the kinetics of epibiont ciliate populations [157, 158].
2.2 Mutualism
Mutualism is a relationship with high metabolic dependence, where both organisms, ciliate and their hosts, obtain benefits [159, 160]. In the phylum Ciliophora, this type of relationship is seen, mainly in the subclass Trichostomatia, which includes the ciliates of the digestive tract of herbivorous mammals [161]. The symbiont ciliates represent approximately 2,600 of the described organisms, of which around 1000 species belong to the subclass Trichostomatia [2]. This subclass comprises ciliated protists, mostly mutualists of the digestive tract of several vertebrate hosts, with only one species showing parasitism in humans, Balantidium coli [2, 162, 163]. The subclass Trichostomatia is divided into three orders: Vestibuliferida, Entodiniomorphida, and Macropodiniida.
Ruminant ciliates and the host have a fundamental symbiosis relationship for the digestion and absorption of large amounts of plant material by the ruminant [164, 165]. On the one hand, the host provides an ideal environment for the survival of the symbiotic microbiota. The rumen is a strictly anaerobic environment, with temperatures ranging from 38 to 41° C, redox potential around 250 to 450 mV (millivolts), osmolarity ranging from 260 to 340 mOsm (millivolts), and pH levels between 5.0 and 7.5. Maintaining these characteristics is essential for microbial enzymatic activity to occur. In return, symbionts provide energy, protein, and vitamins to the host [166]. In energy terms, about 50–70% of the energy obtained by the host comes from the absorption of volatile fatty acids (VGAs) (eg. acetate, butyrate, and propionate), which are absorbed after the breakdown and fermentation of plant fiber by ruminal microorganisms [165]. Ciliates also represent a great source of protein for the ruminant (about 2 to 5%). Still, the ruminal microbiota also synthesizes B and K vitamins in sufficient quantities for the maintenance and growth of the animal. Due to the important participation in the physiology of the ruminant, the evolutionary dynamics of ruminal ciliates has been suggested as closely associated with the radiation of their hosts [167, 168, 169].
2.3 Commensalism and parasitism
Commensalism occurs when the symbiont inhabits in the host with no evident benefit or harm [170].
Parasitism, which is less common in ciliates, involves the parasites that usually cause disease being pathogens. They may be localized or spread throughout a host, defined as the independent and dominant member of the symbiotic pair. Here, the parasite inhabits on or inside the host to obtain resources and to harm it [171].
From an evolutionary point of view, there are species that are entirely free-living, those which can live equally well both free or as symbionts, species that are almost entirely symbiotic with only occasional periods of “free” existence during their life cycles (facultative symbionts), and species which are entirely symbiotic (obligate symbionts). Most of the well documented associations between Ciliophora and Metazoa are the ones leading to a certain degree of metabolic dependence. We will use in this topic the idea of metabolic dependence to define the ecological relationships: “free-living” (no metabolic dependence), “epibiont” (facultative metabolic dependence), “mutualistic” (mutual metabolic dependence) or “parasitic” (unilateral metabolic dependence, including commensalism).
For many years the evolutionary studies for Ciliophora were based only on morphological data, mainly those related to the ultrastructural characterization of its complex infraciliature [2]. However, in recent years this scenario has been modified with the implementation of modern tools that use multidisciplinary methods to integrate morphological, phylogenetic, molecular, and ecological data [161, 172, 173, 174]. A reliably dated phylogeny is fundamental to infer a broad macroevolutionary scenario for Ciliophora [172]. The inference of diversification rates from molecular phylogenies has increasingly been used to derive macroevolutionary patterns of lineages. Understanding how the different ecological relationships evolve in Ciliophora along time is a complex task that has been developed for many years. Different hypotheses about the origin and evolution of parasitic life have been proposed. Parasitologists suggest that the symbiotic way of life probably descended from free-living lineages that subsequently adapted to life in special habitats. Besides this, several authors suggest multiple origins of parasitism based on a comparison of morphological and ultrastructural aspects between them and their free life co-specifics [175], however, the processes that lead to its emergence are still imprecise [176, 177, 178].
Concerning the phylum Ciliophora, the vast majority of ciliates are categorized as free-living, and studies suggested that symbiosis apparently arising independently among various classes [179]. For genus Tetrahymena (subclass Hymenostomatia, order Hymenostomatida), all gradations of adaptations to symbiosis occur. There are species that live totally free, those that can live equally well both free and as symbionts, species that are almost entirely symbiotic with only occasional periods of “free” existence during their life cycles (optional symbionts), and species that are totally symbiotic (mandatory symbionts) [180]. Different transition routes between ecological associations have also been proposed, based on morphological and ecological characteristics. The first one proposes that free-living organisms assume habits of low metabolic dependence (mutualism, commensalism, among others), and with the strengthening of relationships, where they become parasites [176, 181]. The second hypothesis suggests that a free-living organism, when it comes into contact with a host accidentally, adapts itself to live both freely and within that host (optional parasite) [179], that is, free-living organisms adapt to live inside a host, which becomes something advantageous and increases fitness, making this a favorable way of life for the species.
Previous studies aimed to test these hypotheses based on phylogenetic analyzes of small groups within Ciliophora [174, 182, 183]. The macroevolutionary analyzes from the whole Ciliophora phylogeny presented Figure 1 suggested that the ancestral way of life of the ciliates originated from a free-living organism and that the parasitic way of life arose numerous times and independently in Ciliophora, which was induced by two types of ancestors, free life and mutualistic (Figure 1). The transition to the parasitic way of life was recovered from two different origins: 1) a free-living ancestor evolved into a mutualistic organism and, later, to a parasitic organism, and 2) a free-living ancestor evolved into an organism parasite (highest number of cases). There are also cases where there has been a regression in the ciliate’s way of life, where parasite clades evolved to free-living clades (Figure 1).
Figure 1.
Ancestral habit reconstruction for Ciliophora showing the main routes of transitions. Blue: Free-living. Yellow: Mutualism. Red: Parasitism/commensalism.
4. Future perspectives
The analytical improvement for morphological, ultrastructural, molecular, and evolutionary characterizations in Ciliophora culminated in an “Age of Integration”, which several disciplines interact to infer patterns of biodiversity [184]. Although it is an age in full expansion, several gaps often prevent a study of diversity in its diverse areas in a complete way.
We are in a period of the paradigm shift, where Next Generation Sequencing (NGS) techniques have been applied exponentially, and, therefore, it is expected that new discoveries will emerge and new panoramas will be drawn on the diversity of the strains, as well as their respective ecological interactions. The transition from phylogenetic studies to phylogenomics is based on technological progress combined with exponential sequencing of molecular sequences (DNA, RNA), reduced associated costs, increased computational capacity, and improved analytical protocols. It is important to make efforts in studies to expand such technologies to lineages with little sampling in databases. For example, the classes Prostomatea, Oligohymenophorea, Litostomatea, and Phyllopharyngea, which present several examples of symbiosis, do not have available molecular sequences which prevents the evolutionary inferences of these lineages, requiring in the future more studies to refine the evolutionary hypotheses about the phylum. Efforts to expand metataxonomy using metagenomics and metatranscriptome methods have fed the databases exponentially in several lineages, revolutionized the analysis of environmental microbial diversity [175, 185, 186]. In fact, the generation of data for the target sequencing of phylogenetic, metagenomic, and metatranscriptomic markers is now reasonably well established, and several DNA sequencing platforms based on different technologies are currently available as well as different bioinformatics programs for each level of data extraction. However, due to the limited size of the molecular sequences produced by the platforms (~ 500 bp), phylogenetic estimates may be inadequate. With longer readings comes an improved phylogenetic signal, and we show that it is possible to employ a complete phylogenetic signal approach to taxonomically classify sequences and obtain a robust evolutionary structure of environmental diversity. New sequencing technologies such as nanopore sequencing, which offer long reads, improved the phylogenetic signal and more robust taxonomic patterns, can be an alternative in future studies [187].
With the significant increase in the number of available sequences from NGS sequencing, more effective and less subjective methodologies have been proposed to define the limits and number of independent evolutionary entities, to accelerate the biodiversity assessment process. In the last two decades, the field of species delimitation has intensified in relation to the number of methods available. For this, several methodologies have been proposed, based on biological [188], ecological [189], and molecular data [190], in addition to combining phylogenetic theory and population genetics [191, 192, 193]. The use of these methodologies in ciliates performed very recently to delimit organisms of free life, as species of the genus Frontonia, using the mitochondrial gene COX1 [194], species of the genus Spirostomum, using the ITS spacer region genes [195], and COI and 18S markers of the Paramecium genus.
Finally, several authors have emphasized the lack of studies on the distribution and occurrence of ciliates associated with Metazoa in natural conditions and the the lack of information on the ecology and interactions between epibionts and hosts. Few studies are exploring the natural history and complexity of life cycles, which makes it difficult to characterize optional and mandatory relationships. The absence of the characterization of the ciliate at the stage it is in the host, most studies, only in the environment, making it difficult to characterize the life cycle. Relevant information about habitat, life cycle, infection site is rare for Ciliophora [160, 196, 197].
\n',keywords:"Ciliophora, diversity, ecology, macroevolution, morphology, physiology, symbiosis, taxonomy",chapterPDFUrl:"https://cdn.intechopen.com/pdfs/78037.pdf",chapterXML:"https://mts.intechopen.com/source/xml/78037.xml",downloadPdfUrl:"/chapter/pdf-download/78037",previewPdfUrl:"/chapter/pdf-preview/78037",totalDownloads:150,totalViews:0,totalCrossrefCites:0,dateSubmitted:"April 5th 2021",dateReviewed:"July 9th 2021",datePrePublished:"August 12th 2021",datePublished:"May 18th 2022",dateFinished:"August 12th 2021",readingETA:"0",abstract:"Although many ciliates are free-living, more than 140 families of ciliates (Alveolata, Ciliophora) include symbiotic species of animals. Symbiosis, defined as an interaction between two species, is analyzed in this chapter to show a wide diversity of symbiotic systems in ciliates (epibiosis, commensalism, mutualism, and parasitism), providing some data about ciliate strategies showing their success as symbionts. Some species are free-living as well symbionts, facultative symbionts, and obligate symbionts. Analysis of reconstructions of ancestral state evidence that the parasitism arose numerous times and independently among the lineages of ciliates. At least three evolutionary routes can be traced: (1) transition from free-living to mutualism and parasitism, (2) transition from free-living to parasitism, and (3) regression from parasitism to free-living. The evolution of the symbiosis in ciliates demonstrates a higher diversification rate concerning free-living ciliates. The analysis of the evolution of the life cycles complexity, exploring molecular data of the phases of the ciliate cycle in their hosts is also essential. We propose new approaches for an integrative study of symbiotic ciliates.",reviewType:"peer-reviewed",bibtexUrl:"/chapter/bibtex/78037",risUrl:"/chapter/ris/78037",signatures:"Rosaura Mayén-Estrada, Roberto Júnio Pedroso Dias, Mireya Ramírez-Ballesteros, Mariana Rossi, Margarita Reyes-Santos, Carlos Alberto Durán-Ramírez and Gerardo Cruz-Jiménez",book:{id:"10251",type:"book",title:"Plankton Communities",subtitle:null,fullTitle:"Plankton Communities",slug:"plankton-communities",publishedDate:"May 18th 2022",bookSignature:"Leonel Pereira and Ana Marta Gonçalves",coverURL:"https://cdn.intechopen.com/books/images_new/10251.jpg",licenceType:"CC BY 3.0",editedByType:"Edited by",isbn:"978-1-83968-609-2",printIsbn:"978-1-83968-608-5",pdfIsbn:"978-1-83968-610-8",isAvailableForWebshopOrdering:!0,editors:[{id:"279788",title:"Dr.",name:"Leonel",middleName:null,surname:"Pereira",slug:"leonel-pereira",fullName:"Leonel Pereira"}],productType:{id:"1",title:"Edited Volume",chapterContentType:"chapter",authoredCaption:"Edited by"}},authors:[{id:"331546",title:"Dr.",name:"Rosaura",middleName:null,surname:"Mayén Estrada",fullName:"Rosaura Mayén Estrada",slug:"rosaura-mayen-estrada",email:"rme2@ciencias.unam.mx",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/331546/images/system/331546.png",institution:{name:"National Autonomous University of Mexico",institutionURL:null,country:{name:"Mexico"}}},{id:"333204",title:"Dr.",name:"Roberto",middleName:null,surname:"Júnio Pedroso Dias",fullName:"Roberto Júnio Pedroso Dias",slug:"roberto-junio-pedroso-dias",email:"rjuniodias@hotmail.com",position:null,profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0033Y000031SGPDQA4/Profile_Picture_1601626287796",institution:{name:"Universidade Federal de Juiz de Fora",institutionURL:null,country:{name:"Brazil"}}},{id:"357277",title:"MSc.",name:"Mireya",middleName:null,surname:"Ramírez-Ballesteros",fullName:"Mireya Ramírez-Ballesteros",slug:"mireya-ramirez-ballesteros",email:"mballesteros@ciencias.unam.mx",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",institution:null},{id:"357278",title:"Dr.",name:"Mariana",middleName:null,surname:"Rossi",fullName:"Mariana Rossi",slug:"mariana-rossi",email:"mfonsecarossi@gmail.com",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",institution:{name:"Universidade Federal de Juiz de Fora",institutionURL:null,country:{name:"Brazil"}}},{id:"357279",title:"MSc.",name:"Carlos Alberto",middleName:null,surname:"Durán-Ramírez",fullName:"Carlos Alberto Durán-Ramírez",slug:"carlos-alberto-duran-ramirez",email:"carlosduran_88@hotmail.com",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",institution:null},{id:"357280",title:"BSc.",name:"Gerardo",middleName:null,surname:"Cruz-Jiménez",fullName:"Gerardo Cruz-Jiménez",slug:"gerardo-cruz-jimenez",email:"cruzgera16@hotmail.com",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",institution:null},{id:"357281",title:"BSc.",name:"Margarita",middleName:null,surname:"Reyes-Santos",fullName:"Margarita Reyes-Santos",slug:"margarita-reyes-santos",email:"mrsaster@gmail.com",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",institution:null}],sections:[{id:"sec_1",title:"1. 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Consequently, melatonin has beneficial effects including stimulation of antioxidant enzymes, inhibition of lipid peroxidation, and so it contributes to protection from oxidative damages.",book:{id:"7328",slug:"melatonin-molecular-biology-clinical-and-pharmaceutical-approaches",title:"Melatonin",fullTitle:"Melatonin - Molecular Biology, Clinical and Pharmaceutical Approaches"},signatures:"Aysun Hacışevki and Burcu Baba",authors:[{id:"248612",title:"Associate Prof.",name:"Aysun",middleName:null,surname:"Hacışevki",slug:"aysun-hacisevki",fullName:"Aysun Hacışevki"},{id:"248614",title:"Ph.D.",name:"Burcu",middleName:null,surname:"Baba",slug:"burcu-baba",fullName:"Burcu Baba"}]},{id:"75377",title:"Pathophysiologic Approach to Type 2 Diabetes Management: One Centre Experience 1980–2020",slug:"pathophysiologic-approach-to-type-2-diabetes-management-one-centre-experience-1980-2020",totalDownloads:777,totalCrossrefCites:0,totalDimensionsCites:0,abstract:"This overview summarizes the evolution of pathophysiologic treatment of diabetes type 2 (T2D) in the period of the last 40 years. 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This powerful anabolic hormone regulates the transport of glucose into the cell through translocation of glucose transporter from an intracellular pool to the plasma membrane mainly in metabolically active tissues like skeletal muscles, adipose tissue, or liver (GLUT4). This translocation occurs through multiple steps of PI3K/AKT signaling pathway. In this chapter, we will focus on molecular events leading to GLUT4 translocation, starting with activation of insulin receptors through signaling cascade involving phosphatidylinositol 3-kinase (PI3K) and protein kinase B (PKB) and finally, the action of their effectors. 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The poor long- and short-term perinatal and postnatal results associated with this context make it necessary to establish an early diagnosis and a therapeutic strategy, which can be challenging due to the compromise between the threat of intrauterine permanence and the prematurity problem. 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He completed a one-year Post-Doctoral Fellowship awarded by the DFAIT (Foreign Affairs and International Trade Canada) at the Institute of Biomedical Engineering of the University of New Brunswick (Canada) in 2010. Currently, he is Professor in the Faculty of Electrical Engineering (UFU). He has authored and co-authored more than 200 peer-reviewed publications in Biomedical Engineering. He has been a researcher of The National Council for Scientific and Technological Development (CNPq-Brazil) since 2009. He has served as an ad-hoc consultant for CNPq, CAPES (Coordination for the Improvement of Higher Education Personnel), FINEP (Brazilian Innovation Agency), and other funding bodies on several occasions. He was the Secretary of the Brazilian Society of Biomedical Engineering (SBEB) from 2015 to 2016, President of SBEB (2017-2018) and Vice-President of SBEB (2019-2020). He was the head of the undergraduate program in Biomedical Engineering of the Federal University of Uberlândia (2015 - June/2019) and the head of the Centre for Innovation and Technology Assessment in Health (NIATS/UFU) since 2010. He is the head of the Postgraduate Program in Biomedical Engineering (UFU, July/2019 - to date). He was the secretary of the Parkinson's Disease Association of Uberlândia (2018-2019). Dr. Andrade's primary area of research is focused towards getting information from the neuromuscular system to understand its strategies of organization, adaptation and controlling in the context of motor neuron diseases. 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