Released this past November, the list is based on data collected from the Web of Science and highlights some of the world’s most influential scientific minds by naming the researchers whose publications over the previous decade have included a high number of Highly Cited Papers placing them among the top 1% most-cited.
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We wish to congratulate all of the researchers named and especially our authors on this amazing accomplishment! We are happy and proud to share in their success!
IntechOpen is proud to announce that 191 of our authors have made the Clarivate™ Highly Cited Researchers List for 2020, ranking them among the top 1% most-cited.
\n\n
Throughout the years, the list has named a total of 261 IntechOpen authors as Highly Cited. Of those researchers, 69 have been featured on the list multiple times.
\n\n\n\n
Released this past November, the list is based on data collected from the Web of Science and highlights some of the world’s most influential scientific minds by naming the researchers whose publications over the previous decade have included a high number of Highly Cited Papers placing them among the top 1% most-cited.
\n\n
We wish to congratulate all of the researchers named and especially our authors on this amazing accomplishment! We are happy and proud to share in their success!
Note: Edited in March 2021
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\r\n\tNephritis can be seen as hereditary or as a result of infection, immunological diseases, metabolic disorders, exposure to toxic factors, and glomerular or hematological diseases. It may be asymptomatic or accompanied by hypertension, renal tubular acidosis, proteinuria, hematuria, edema, anemia, glucosuria, and nocturia. It is a progressive and chronic disease with sometimes acute exacerbations. Chronic nephritis often leads to chronic kidney disease, causing tubular atrophy and interstitial fibrosis. It is seen in approximately 15% of the causes of end-stage kidney disease. Generally, the pathological findings are tubular atrophy and dilatation, fibrosis in the interstitial space, and inflammatory cell infiltration, mostly consisting of mononuclear cells. In the later stages of the disease, glomerulosclerosis and vascular sclerosis develop. Current treatment involves diagnosing and eliminating the causative factor of chronic interstitial nephritis and treating complications according to the extent of kidney damage, the treatment of chronic nephritis is difficult, and the prognosis is poor; treatment is aimed at the etiology. The search for antifibrotic treatment continues in experimental models; various hormones, immunosuppressants, and symptomatic treatments are given according to the degree of renal damage and complications. However, since these treatments are applied for a long time, they cause many complications in the patient.
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\r\n\tNephrotic syndrome is one of the most common chronic diseases of childhood in which many symptoms due to kidney damage are seen together. Massive proteinuria, hypoalbuminemia, hyperlipidemia, lipiduria, and edema are observed in the patient's clinic. 90% of childhood nephrotic syndrome cases are due to primary idiopathic or minimal change disease. It is often seen in adults due to focal segmental glomerulosclerosis, membranous nephropathy, lupus, or diabetes. \r\n\tWhile histopathologically, the most common minimal change disease is focal segmental glomerulosclerosis, membranoproliferative glomerulonephritis, mesangial proliferation, proliferative glomerulonephritis, and membranous glomerulopathy can be seen. Treatment is planned according to symptoms, complications, and primary disease. The first goal is to minimize protein loss. Although corticosteroids are the first choice in treatment, if side effects occur or the disease does not respond, immunosuppressive treatments are applied. Current treatment approaches have shown promising results in terms of disease treatment. However, its long-term side effects and remission sustainability are still unclear.
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\r\n\tNephrosis is an inflammatory, neoplastic or non-vascular nephropathy that causes degenerative changes and solute accumulation in tubules and glomeruli. Nephrosis may be due to a primary cause or secondary to another disorder. Nephrosis is often seen as amyloid nephrosis and osmotic nephrosis. Osmotic nephrosis causes structural changes with intracytoplasmic vacuolization and swelling of tubular cells, occurring primarily in the proximal tubules, without a change in osmotic balance, resulting from certain solutes such as dextran, contrast dyes, mannitol, and hydroxyethyl starch. It can lead to clinical manifestations ranging from acute renal failure to chronic kidney disease. \r\n\tAmyloid light-chain amyloidosis is the most common type of amyloidosis, with the kidney one of the organs most commonly affected. With the enlargement of the kidney area affected by amyloid deposits, proteinuria and renal dysfunction are usually observed. This topic includes advances in research on the etiology and pathogenesis of nephritis, nephrotic syndrome, and nephrosis, new early diagnosis methods, follow-up and treatment plans, and case series. It will provide significant opportunities and support to scientists, philosophic and medical doctors, urologists, nephrologists, public health practitioners, and family physicians from around the world to share new research, ideas, and solutions.
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1. Introduction
The pregnancy and the adaptation to motherhood is one of the most signifcant events during a woman’s life time. The pregnancy is associated with major psychological and physical changes. The woman expects to attach to the fetus and prepare for the life as a mother. Interventions during pregnancy must be implemented with respect for the sensitive period as a pregnancy is.
The aim with this chapter is to describe and discuss possible effects of prenatal examinations for Down syndrome during pregnancy on maternal-fetal attachment. Additional aims are to illuminate experiences and reactions during the waiting-time for test results, the experience of false positive results from screening examinations and the perception of complex information from prenatal examinations.There is of great importance to explore and highlight these questions to minimize the risk for negative affection on the maternal-fetal attachment by prenatal screening or diagnosis for Down syndrome.
2. Maternal-fetal attachment
One of the basic prerequisite for the survival of a new-born baby is that there is a relation of attachment to the parents. This means a lasting emotional relation to a person who will secure the baby’s trust and safety. The theory about attachment was developed by John Bowlby in England in the 50s. Maternal-fetal attachment (MFA) is a concept used to describe the relationship between a pregnant woman and the fetus. It describes the process in which the pregnant woman experience feelings and emotions for the fetus. At the same time her maternal identity is developed. This concept is rather new and is still not well studied or fully defined. MFA is based on representations of the fetus according to qualitative descriptions of maternal attitudes and adaption to pregnancy (Salisbury et al., 2003). The attachment between the pregnant woman and the fetus during the pregnancy had been described as the first important relation to the baby and has strongly been associated with the following mother-child relation after the birth. The attachment to the fetus and later to the baby is developing successively. It starts in early pregnancy and increases during the pregnancy to be most intensive during the last trimester (Alhausen, 2008, Yercheski, 2008). The concept maternal-fetal attachment was defined by professor Mecca S. Cranley and are described as “the extent to which women engage in behaviors that represent affiliation and interaction with their unborn child” (Cranley, 1981, s 282).
There is not consensus about the concept attachment/bonding during pregnancy. The definitions are in generally split in definitions which describe attachment as emotions and those who describes attachment as behaviours during pregnancy which indicates the pregnant woman’s attachment to the fetus. Three scales based on each definition of the concept have been developed to quantify MFA. The original maternal-fetal attachment scale (MFAS), developed by Cranley (1981) contains 24 items and intends to measure maternal-fetal attachment. The scale measures to what extent the mother-to-be is engaged in behaviour which is expressing a sense of belonging and an interaction with the unborn baby. The attachment is defined as how the mother-to-be cope with the development as the pregnancy means. It was developed from the attachment theory of Bowlby (Bowlby, 1969). The 24 items were divided into five subscales; differentiation of self from fetus, interaction with the fetus, attributing characteristics to the fetus, giving of self, and role taking. The response format is Likert-like with scores of 1 (definitely no), 2 (no), 3 (uncertain), 4 (yes) and 5 (definitely yes). Regarding the reliability of the scale, in previous studies. In previous studies the Cronbach’s alpha for the total scale ranged from .82 to .91 and for the subscales .52 to .73 (Bloom, 1995; Lindgren, 2001; Shieh, 2006).
In 1990 another, the second, instrument intending to measure prenatal attachment was developed by Müller. This instrument – prenatal attachment inventory(PAI) was designed to measure the relationship that develops between the mother-to-be and the fetus. Müller defined prenatal attachment as the unique, affectionate relationship that develops between the pregnant woman and the fetus (Müller, 1993).
According to Condon &Corkindale, 1997, the concept prenatal attachment include the following five factors; wishing for knowledge about the unborn baby, happiness for the interplay with the baby, wishing for protecting the baby and satisfying its needs, worrying about losing the baby or that something will be wrong with the baby, and that the baby’s needs have priority over the own needs. They developed the instrument MAAS (maternal antenatal attachment scale). Condon’s definition was closer to the attachment theory of Bowlby. Condon described attachment as love, his definition of attachment was “the core experience of attachment is love” and proposed five subjective experiences of love.
There are some difficulties to measure maternal-fetal attachment with the self assessment instruments which are available today. One difficulty is the limitation of the scales in their sensitivity to cultural differences and experiences. An adaption of the existing scales may be possible. Cranley’s maternal-fetal attachment scale has been modified to a Japanese version with 20 items. The results of that study of 275 women confirmed previous studies. MFA increased significantly from gestational week 5 to gestational week 40. Feeling fetal movements had a particularly positive effect. Women with ambivalent feelings responded lower in the scale (Narita &Maehara, 1993).
Another close concept to maternal-fetal attachment is maternal/fetal interaction. A questionnaire to measure maternal/fetal interaction was developed in 1997 by Nelson. By this instrument the mothers spontaneous talk to herself or to the fetus assessed and emotional words such as “happy”, “sad”, “bored”, “excited”, “calm” or “anxious”. Higher scores on the scale indicate higher level of maternal/fetal interaction (Ji& Han, 2010).
3. Factors which may affect maternal-fetal attachment
The development of the technologies which are used in the context of pregnancy and child birth may have psychological consequences for the expecting mother. There are normal psychological changes during pregnancy. It is a period of psychological and physiological adaptation and causes strong emotional reactions and sometimes even ambivalent feelings. It is a complex process. It is also related to the partner, the own mother and friends (Bibring et al., 1961; Shereshefsky& Yarrow, 1975). The first part of a pregnancy is characterized as a vulnerable period when the woman has to accept the fetus as a part of herself (Raphael-Leff, 1992). All interventions during pregnancy must be done with the normal psychological changes in mind.
Some factors are known as such which may facilitate the attachment; the experience of fetal movements, support from family, friends and the partner. Higher age of the expectant mother, depression, worry and abuse may affect the attachment in a negative way. Higher levels of maternal-fetal attachment are reported when the woman has a positive relationship with the expectant father. Women with high- risk pregnancies do not seemed to attach to their fetus in a lower extent than women with normal pregnancies.Failure to attach to the fetus during pregnancy seems to be more common in women from poor social and economic conditions (Alhausen, 2008). Patient education courses seem to positively influence the prenatal attachment (Bellieni et al., 2007).
In a study of 252 pregnant women MFA had a positive relationship with positive health practices, such as diet exercise, drug and alcohol use (Lindgren, 2001).The author discuss the practical problems about interventions intended to increase maternal-fetal attachment. There is not yet evidence which effects different interventions have on MFA. However, some reasons for delayed or low levels of maternal-fetal attachment are well-known, for example self-protection for emotional trauma suffering during a previous loss. In the antenatal care the care givers can try to identify women with poor maternal-fetal attachment and help them improve their health practices trying to improve woman’s health and pregnancy outcome.
Effects of an intervention based on mind and body interconnectedness, called Qi, on maternal-fetal interaction were studied. Totally 70 women were included in the study. Qi exercise was carried out in the second half of the pregnancy. The exercise lasted for 90 minutes, twice a week. This study showed effect of Qi on maternal/fetal interaction as well as on maternal depressive symptoms and physical comfort. In this study the maternal/fetal interaction was measured by the Interpersonal Communication Questionnaire (Talking to the baby) ( Ji & Han, 2010).
Hyperemesis gravidarum is a rather rare complication of pregnancy, which means a severe form of nausea and vomiting. This may lead to problems to intake food and fluid. Among women with hyperemesis gravidarum there were an association with less developed maternal-fetal attachment in gestational weeks 7-16, but this negative effect was very small compared to pregnant women without hyperemesis gravidarum. At follow-up after 26th weeks of gestation this negative effect could not be proved anymore (McCormack et al., 2011).
Maternal-fetal attachment is not studied in developing countries. It is reasonable to assume that the MFA is affected of the high mortality rate for both women and infants (Salisbury et al., 2003).
When using assistance with IVF – in vitro fertilization to get pregnant there may be stressful for the woman compared to getting pregnant the “normal” way. However, it does not seem to affect the attachment to the baby during pregnancy (McMahon et al., 1997, Stanton &Golombok, 1993). Prenatal attachment was in a study by Hjelmstedt and colleagues (2006) compared between 56 women who had underwent IVF and 41 controls. A self-rating scale was completed in gestational weeks 26 and 36. As the pregnancy progressed the prenatal attachment was increased in the same way in both groups. A conclusion of this study was that marital satisfaction, age, ambivalence and detachment was significant contributors to prenatal attachment. As proved in other studies the same results are presented regarding women who get pregnant with assistance. When women are less positive about pregnancy, childbirth and childcare they show weaker attachment to their unborn child (Stanton &Golombok, 1993).
When having an increased risk for having a child with a genetic condition one possibility is PGD (prenatal genetic diagnosis). In vitro fertilization is used to produce embryos which are genetic tested and selected on the absence of particular genetic conditions. There is often a need for repeated cycles of ovarian stimulations, IVF and transfers of an embryo. This is trying and results in fluctuations in the woman’s anxiety (Karatas et al., 2011), which may affect the attachment.
4. Prenatal examinations in generaland its possible effects on maternal-fetal attachment
An ultrasound examination in the second trimester is offered to all pregnant women in Sweden. This examination is accepted of the vast majority (SBU 1998). To many expecting parents the ultrasound examination has such a strong confirming effect that they wait until after the examination before they tell family and friends about the pregnancy (Ekelin, 2004). The possibility to see the fetus on the ultrasound screen has shift the focus from the time point when the pregnant woman felt the movements of the baby by herself to the time point when you can see the fetus on the screen.
If, and in what extent, prenatal examinations affects the attachment are fairly insufficient explored. Ultrasound examination usually takes place before the woman recognizes the first movements of the baby and may be a facilitator for maternal-fetal attachment. However, studies of ultrasound examination and its effects on the maternal-fetal attachment show contradictory findings. The relationship between the expectant mother, and even the expectant father may start earlier in pregnancy (Stormer, 2003, Zeichmeister, 2001). The time point when the woman reported movements from her baby, so called quickening, used to be a very important moment, but have in those days been replaced by seeing the fetus on the ultrasound screen. Studies of attachment between the expecting mother and the fetus in relation to ultrasound examination have showed contradictory results (Lumley, 1990). Some studies do not present any differences between the attachment to the fetus (Heidrich & Cranley, 1989), whereas other studies present a positive effect (Caccia, 1991), especially the first ultrasound examination during pregnancy (Sandbrook& Adamson-Macedo, 2004) and ultrasound examination early in pregnancy (Stormer, 2003). According to a meta-analysis of the effects of ultrasound examination on maternal-fetal attachment, the attachment increased to some extent (Yercheski et al., 2008). Several studies of the effects of 3D- or 4 D ultrasound have not proved any improved attachment compared to 2 D ultrasound (Righetti et al., 2005; Rustico et al., 2005, Sedgmen et al., 2005), but may cause a positive change in the parents-to-be’s feelings for the fetus (Pretorius et al., 2006). The attachment seems to increase and the worry about the health of the fetus decrease when the ultrasound examination is combined with a discussion with a health care professional. The discussion contained an explanation of the woman’s and the fetuses anatomy and a demonstration of fetal movements. Except the discussion in relation to the examination the strategy also contained a follow-up discussion (Boukydis et al., 2006). When assessing the ultrasound examination’s effects on the maternal-fetal attachment there are, except the general difficulties to measure maternal-fetal attachment, some methodological factors to take into consideration. The length of the examination, the information related to the examination and the communication between the health care giver and the parents-to-be affects the experience of the examination and may even the maternal-fetal attachment (Alhausen, 2008). Comparing studies are difficult to perform due to the fact that almost all women undergo ultrasound examination during pregnancy (Lumley, 1990).
The aim of an ultrasound examination in the second trimester is not primarily screening for Down syndrome but it is possible to detect malformationssoft markers or anomalies which are associated with Down syndrome.
5. Prenatal examinations for Down syndrome and its possible effects on maternal-fetal attachment
Today, many of the prenatal examinations and screening such as nuchal translucency measurement in early pregnancy, maternal serum screening, combined ultrasound examination and biochemical screening and invasive diagnostics are aimed to find risk pregnancies for Down syndrome or Down syndrome. The invasive test being used are amniocentesis or chorion villousbiospy. To be offered early screening, either early ultrasound examination including measurement of nuchal translucency or maternal serum screening has in one study showed an increase of the maternal-fetal attachment. However, this increase seemed to be small and temporary (Kleinveld et al., 2008). A conceivable reason that the attachment will increase may be that the women receive information about the examination which lead to improved awareness about the unborn baby. The awareness will, of course, be improved if the woman undergoes the examination. Even following invasive test may the attachment to the fetus increase. Among women who underwent chorion villus biopsy the attachment increased five week earlier than for those who underwent amniocentesis. When the women received normal test results the attachment increased. However, there are even results from studies which show the opposite. Women who had underwent serum screening on the indication advanced maternal age showed less attachment than those who underwent amniocentesis for the same indication or those who refused the test. The reason for that may, due to the discussion by the authors, that screening do not result in a diagnosis but a probability for Down syndrome which may lead to an additional feeling of insecurity (Lawson & Turiff-Jonasson, 2006).
There is insufficient research in the field of how risk or perceived risk for the baby during pregnancy influences the MFA. One study which had the underlying assumption that women in high risk groups would have less MFA than women in low-risk groups failed to proved that (Cannella, 2005). In a qualitative study by Hedrick (2005) of women who expected a child with a nonlethal abnormality, the participants did not express less maternal fetal attachment, rather a feeling of a wish to protect the baby who was not perfect. However, information about an increased risk for carrying a baby with Down’s syndrome from an early ultrasound examination including nuchal translucency measurement strongly implies the worry about the baby (Georgsson Öhman et al., 2006).
In a sub study of large randomized controlled trial aiming at evaluating the effects of screening for Down syndrome by means of an ultrasound scan including measurement of nuchal translucency in early pregnancy (gestational weeks 12 to 14), the aim was to investigate how the early scan compared to a ultrasound examination in second trimester, may have affectedmaternal-fetal attachment in mid-pregnancy. There were 2026 women included in the study. Women were randomly allocated either o the intervention or to a control group where the routine care with an ultrasound scan in gestational week 17 to 20 was offered. Data were collected by questionnaires before randomization and in gestational week 24. MFA was measured by a modified version of the Cranleymaternal-fetal attachment scale. One item (I grasp my baby’s foot through my tummy to move it around) was excluded in the present study because it seemed irrelevant to use in gestational week 24. Another item (I enjoy watching my tummy jiggle as the baby kicks inside) was replaced with “I like to read about the development of the baby, how it grows, how it looks like”. Mean scores were used for comparisons and were calculated for the total scale and individual subscales. The results of the study showed that the mean score of MFA was 3.50 in the intervention group compared to 3.44 in the control group (p=0.04). The mean scores on all subscales were slightly higher in the intervention group, but only statistically significant regarding “Differentiation of self from fetus” p = 0.01. The conclusion of this study was that ultrasound screening for Down syndrome in the first trimester may have a modest positive effect on MFA in mid-pregnancy, compared with a ultrasound scan in the second trimester (Georgsson Öhman & Waldenström (2010).
In a study by Berryman and Windridge (1996) a lower attachment to the fetus among older women was shown. The authors interpreted this result as they restrain the attachment because they were aware about the risk of Down syndrome associated to high maternal age and as a consequence a possible loss of the pregnancy.
6. Reactions and experiences during waiting-time for test results
To wait for results from invasive testing, such as amniocentesis and chorionvillousbiopsy, seems to be worrying and a period full of concerns. This seems to be a difficult time period irrespective of nothing is expected to deviate, and irrespective of the invasive test has preceeded of information about increased risk for chromosomal abnormalities or not (Cederholm et al., 2001). Women who have undergone an amniocentesis described that they had an emotional distance to the pregnancy until the health of the fetus had been confirmed by the result of the test (Rothman, 193). The waiting time are often experienced as hard irrespective of normal test result or not (Cederholm et al., 2001, Green & Statham, 1996).
Manywomen who had received information about risk for the fetus having Down syndrome in relation to an early ultrasound examination including nuchal translucency measurement, describes the waiting time for having an amniocentesis and further to wait for the test result as a time when they repressedthe pregnancy. They avoided to think about the baby, and denied their pregnancy in different ways. This can be interpreted as a strong feeling but still the question if this period of repression of the pregnancy affects the attachment is unanswered. Information about increased risk for something being wrong with the baby may lead to great consequences for the pregnant women, such as denying the pregnancy - taking a “time-out”, until the test shows normal results. The women did not feel happiness about the pregnancy, they didn’t tell anyone about it, didn’t look for baby equipment or thought about names for the baby. This “time-out” lasted until a normal result from the invasive test was received in about one month. Considering one month of denying the pregnancy it is still reasonable to assume that prenatal examinations may affect the attachment (Baillie, 2000; Georgsson , Öhman et al., 2006).
7. False positive results
To receive false positive results that there is an increased risk for the baby having a chromosomal abnormality lead to unnecessary worry about the health of the baby. Women have describes the time from receiving an increased risk that the baby have Down syndrome until they receive a normal result from the invasive test as a “time-out”a repression of the pregnancy as mentioned above (Baillie et al., 2000; Georgsson, Öhman et al., 2006). There are reasons to assume that this time with decreased interaction with the fetus may affect the attachment and the feelings for the unborn child in some way. This is an important question for further research. Including waiting-time for the invasive test and the test result this period when the women repressed pregnancy could last for about a month.
In general, to reduce the number of false positive results is an important ethical issues about screening. Even after a reassuring diagnostic test can some worry remain (Green et al., 2004). In a study by Baillie et al. (2000), 24 women who received a false positive result from an ultrasound examination including measurement of nuchal translucency and a calculation of the probability for having a baby with Down syndrome were interviewed. Two thirds of the women in the study still experienced anxiety up to four weeks following the normal diagnostic test. In a study by Weinans and colleagues in 2004 anxiety in association with false positive results from nuchal translucency screening and from serum screening was compared. There were 20 women in each group in both groups the risk was presented as a numerical value. In this study the women in the group who underwent nuchal translucency screening stated they were more worried about the health of the baby than those who underwent maternal serum screening. A possible explanation to this finding is that the fetus was visualized in the “NT-group”. In a study including 33 women who received false positive results from serum screening, 20% remained worried two months after a normal diagnostic test (Santalahti et al., 1996). Feelings of worry could easily be recalled as long as ten years after maternal serum screening (Smedler&Bremme, 1992). In a study of 102 families who had received false positive results from screening for congenital hypothyreoidism, 78 families experienced strong emotional reactions. As many as 18 of these families stated that they still felt insecure about the baby’s health after a period of 6 to 12 months (Bodegård, Fyrö& Larsson, 1983). This link of studies presented above, all show that false positive results make a deep mark on those who are affected. There are still no studies which explore the effect of those strong feelings on the maternal fetal attachment.
8. Importance of information
Information about prenatal screenings and diagnostic is very complicated and complex. To give equal information in early pregnancy to all women who want to have the information is a great challenge. The ambition is to give equal information to all women irrespective of social and cultural background, education and age. The information will be standardize, evidence based, comprehensible and not generate worry (SFOG, 2008).
The content of the information will be;
that most of the newborn children are healthy,
the purpose with the screening or the examination,
the pros and cons,
that the participation is voluntary
about the methods – the procedure, possibilities, limitations
that a assessment of probability is not a diagnosis
the meaning of the test results
the probability for false positive and false negative results
possible consequences and possible alternatives after the test results
that the parents-to-be will be faced difficult decisions and dilemmas in cases were a abnormality is detected
how common the abnormalities are and possible consequences for the child
The aim with the information about prenatal diagnosis is to enable the woman to make an informed choice (Dormandy et al., 2002). One common definition of informed choice adapted from O’Connor et al. (2009) is that “the informed choice is based on relevant knowledge, consistent with the decision makers’ values and behaviourally implemented”. When talking about prenatal screening or diagnosis this means that an informed choice to undergo prenatal examinations is when the woman has relevant knowledge about the test, a positive attitude towards it and actually undergoes it (Marteau et al., 2001, Michie et al., 2002, Potter et al., 2008). Sufficient knowledge is not enough to be able to make an informed choice. The choice should also reflect one’s values and attitudes towards undergoing the test.
There are several difficulties with information regarding prenatal examination. Many pregnant women do not know that prenatal screening is an option; they do not know the meaning of false positive and false negative results and what it means to live with DS but they have more knowledge of practical aspects of prenatal screening (Dahl et al., 2008). Pregnant women can receive information about prenatal screening from different sources such as health care, pamphlets, books, the internet, friends and family (Park & Matthews, 2009). Film as a source of information has shown to increase the knowledge (Björklund et al., 2011, Hewison et al., 2001).
Regarding information about prenatal screening, a study was performed with the aim to compare the growth of maternal-fetal emotional attachment in groups of women whose decisions about participation in screening were informed or not informed. The result of the study showed that the group who made an informed choice had significantly lower attachment scores than the group who had not made an informed choice. The authors pointed out that the findings of this study have uncertain consequences. Delayed emotional attachment can be interpreted as a psychological defense, a way to keep distance from the fetus in case if the pregnancy will be terminated due to diagnosis of fetal abnormality (Rowe, 2009). Delayed attachment may prevent positive behaviour which protects well-being of both the woman and the fetus such as good diet; non smoking and alcohol use (Rowe et al., 2009). On the other hand is it an important purpose in the antenatal care to strive for so many women as possible to been able to make an informed choice (Halsey Lee et al., 2005).
9. Conclusion
The human being is malleable and most difficulties and crisis we are able to cope with. Despite traumatic experiences, such as information about something may be wrong with the baby, with following crisis and repressing of the pregnany most of the women seem to recover and develop a stromg attachment to the fetus and bonding to the new born baby. However, some women may show stronger reactions such as depression or considerable worry. There is also a risc for remaining distrustfulness for the health of the child during the childhood. So far, there is a lack of concordant methods to measure maternal-fetal attachment, with some contraditiry results from research. Further development, validation and assessment of the available scales for self assessment of matrnal feta attachment are in a great demand. Further research is required to verify possible effects of prenatal examinations on the maternal fetal attachment in general. Additionally, there is a need for scrutinizing the field of information, and the possibility for the expectant mothers to make an informed choice regarding prenatal examinations. There is a lack of knowledge about conceivable adverse effects of prenatal examinations for detecting Down syndrome during pregnancy.
\n',keywords:null,chapterPDFUrl:"https://cdn.intechopen.com/pdfs/17998.pdf",chapterXML:"https://mts.intechopen.com/source/xml/17998.xml",downloadPdfUrl:"/chapter/pdf-download/17998",previewPdfUrl:"/chapter/pdf-preview/17998",totalDownloads:3460,totalViews:188,totalCrossrefCites:1,totalDimensionsCites:1,totalAltmetricsMentions:0,introChapter:null,impactScore:1,impactScorePercentile:54,impactScoreQuartile:3,hasAltmetrics:0,dateSubmitted:"November 3rd 2010",dateReviewed:"May 20th 2011",datePrePublished:null,datePublished:"August 17th 2011",dateFinished:null,readingETA:"0",abstract:null,reviewType:"peer-reviewed",bibtexUrl:"/chapter/bibtex/17998",risUrl:"/chapter/ris/17998",book:{id:"479",slug:"prenatal-diagnosis-and-screening-for-down-syndrome"},signatures:"Susanne Georgsson Öhman",authors:[{id:"34468",title:"Dr.",name:"Susanne",middleName:null,surname:"Georgsson Oehman",fullName:"Susanne Georgsson Oehman",slug:"susanne-georgsson-oehman",email:"susanne.georgsson@ki.se",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",institution:{name:"Karolinska Institute",institutionURL:null,country:{name:"Sweden"}}}],sections:[{id:"sec_1",title:"1. Introduction",level:"1"},{id:"sec_2",title:"2. Maternal-fetal attachment",level:"1"},{id:"sec_3",title:"3. Factors which may affect maternal-fetal attachment",level:"1"},{id:"sec_4",title:"4. Prenatal examinations in generaland its possible effects on maternal-fetal attachment",level:"1"},{id:"sec_5",title:"5. Prenatal examinations for Down syndrome and its possible effects on maternal-fetal attachment",level:"1"},{id:"sec_6",title:"6. Reactions and experiences during waiting-time for test results",level:"1"},{id:"sec_7",title:"7. False positive results",level:"1"},{id:"sec_8",title:"8. Importance of information ",level:"1"},{id:"sec_9",title:"9. Conclusion",level:"1"}],chapterReferences:[{id:"B1",body:'AlhausenJ. L.2008A literature update on maternal-fetal attachment.JOGNN, 37315328'},{id:"B2",body:'BaillieC.SmithJ.HewisonJ.MasonG.2000Ultrasound screening for chromosomal abnormality: women’s reactions to false positive results. 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J PsychosomObstet Gynecol., 1421538'},{id:"B57",body:'StormerN.(20032003Seeing the fetus: The role of technology and image uin the maternal-fetal relationship. Journal of the American Medical Association, 289,1700.'},{id:"B58",body:'RighettiP. L.Dell’AvanzoM. D.GrigioM.NicoliniU.2005Maternal/paternal antenatal attachment and fourth-dimensional ultrasound technique: a preliminary report. British Journal of Psychology, 96129137'},{id:"B59",body:'RusticoM. A.MastromatteoC.GrigioM.MaggioninC.GregoriD.NicoliniU.(20052005Two-dimensional vs. two-plus four dimensional ultrasound in pregnancy and the effect on maternal emotional status.A randomized study. Ultrasound ObstetGynecol, 25468472'},{id:"B60",body:'WatsonM. S.HallS.LangfordK.MarteauT. M.2002Psychological impact of the detection of soft markers on routine ultrasound scanning: a pilot study investigating the modifying role of information. Prenatal Diagnosis, 22(7), 569-75.'},{id:"B61",body:'ZeichmeisterI.2001Foetal images: The power of visual technology in antenatal care and the implications for women’s reproductive freedom. Health Care Analysis, 93387400'},{id:"B62",body:'YercheskiA. MahonN.E. YercheskiT.J. HankM.M. CannellaB.L. (2008). A meta-analytic study of predictors of maternal-fetal attachment.Int Journal of Nursing Studies, doi:10.1016/j.ijnurstu.2008.10.013.'}],footnotes:[],contributors:[{corresp:"yes",contributorFullName:"Susanne Georgsson Öhman",address:"",affiliation:'
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Metaheuristic Tabu Search Optimization Algorithm: Applications to Chemical and Environmental Processes",doi:"10.5772/intechopen.98240",slug:"a-metaheuristic-tabu-search-optimization-algorithm-applications-to-chemical-and-environmental-proces",body:'
1. Introduction
Tabu search is a meta heuristic problem solving approach used to solve combinatorial optimization problems. It was first proposed by Glover [1] and further developed by Hansen [2]. TS has now become an established search procedure and has been successfully applied to solve a wide spectrum of optimization problems [3, 4, 5, 6, 7, 8, 9].
1.1 Basic principle
TS uses a memory which allows it to remember the current best solution and also enables it to explore the previous solutions and to direct the search moves. The features of memory adaptation and exploration facilitate TS to find better solutions and discover new potential regions in the search space. The memory adaptation feature helps to realize its course of action to exploit the search space efficiently. The ability of TS to explore good solutions enables it to assimilate the intelligent search mechanisms to search for good solutions and to discover new potential regions. The use of adaptive memory helps TS to learn and creates a more flexible and effective search strategy compared with memory less methods, such as simulated annealing (SA) and genetic algorithms (GA).
1.2 Components of TS
The components of TS are explained as follows.
1.2.1 Neighbors generations and neighborhood search
To optimize the function f(x) globally from all the probable solutions x∈X in the space X, it requires to specify a structure in the vicinity of the solution space and the staring solution. The search advances to alter the existing solution to create a set of promising solutions in the vicinity of solution space. During the search process, the number of solutions traversed by TS is the product of the number of solutions in the vicinity of the solution space, N(xi), and the number of iterations, k. The function at each iteration is evaluated for N(xi) solutions. The better move is chosen in the vicinity of the complete solution space. The search proceeds to the next iteration, to find a solution in the vicinity of the accepted move. Thus, the TS builds a set of viable solutions by using a history record of the search.
1.2.2 Tabu list
The tabu list in TS maintains the data of the previously visited solutions. The list is included with the latest moves and it is altered dynamically as the search proceeds. The data in the tabu list helps to direct the move from the present solution to the next solution. At each iteration, the search process is maintained by updating the tabu list. The tabu list also avoids re-visiting of recent neighbors recorded in the list and thus save computational time.
1.2.3 Short-term memory and long-term memory
The information is stored in tabu list as recency-based short-term memory (RSM) and a frequency-based long-term memory (FRM). When the search proceeds, the nearly better solution to the present solution is sorted as tabu, and added to the recency-based tabu list. As fresh solutions enter the list, older solutions are removed from the bottom. Long-term memory relies on the frequency of a solution that is visited. When the tabu list is filled with the highest number of elements in the frequency based tabu list, the solution with the smallest frequency index will be replaced.
1.2.4 Intensification and diversification
These strategies are used to create neighbors that have higher likelihood of finding optimal solutions based on the data in the tabu list. Intensification strategies are used to search potential areas in detail around the areas that are found good in the past. Intensification strategies are generally employed based on long term memory whose components are used to create neighbors for search intensification [4, 6, 10]. Diversification strategies are used to search the complete viable region, thus restricting the search getting trapped in local optima. These strategies promote probing unvisited regions by creating solutions radically different from those searched earlier [4]. A frequency-based tabu list is used to keep track of the search area.
During the generation of neighbor solutions, the difference between the present and fresh neighbor solution is managed by using a coefficient, α. The change from the current point is multiplied by α during the course of building new neighbors. The coefficient α is in the form of a sine function [10].
α=121+siniθπNneighE1
Here i is index of the neighbor, Nneigh is the total number of neighbor solutions generated at each iteration, and θ is a parameter that controls the oscillation period of α.
1.2.5 Aspiration criterion
The TS conditions at times prevent moves leading to unvisited solutions. Aspiration criterion is a condition that can override the tabu status of a certain move. To avoid certain missing solutions during the search, the aspiration criterion in certain cases may invalidate the tabu property and maintains an appropriate balance between diversification and intensification [4, 10, 11].
An aspiration criterion that is designed based on a sigmoid function as given by
Sk=11+e−σk−kcenter×ME2
where kcenter, k, σ and M denote the tuning parameter, current iteration number, another tuning parameter and maximum number of iterations. The value of kcenter can be in the range of 0.30–0.70, the value of σ can be in the range of 5/M to 10/M. A random number P that lies between 0 and 1 is generated from a uniform distribution at each iteration. If P is greater than S(k), the tabu property is active and the best non-tabu neighbor is used as a fresh starting point. If P is less than or equal to S(k), the aspiration criterion ignores the tabu property.
1.2.6 Stopping criteria
A stopping criterion is needed to terminate the search when the optimum is reached. The stopping criterion can be in the form of fixing the number of iterations or specifying a threshold for convergence of solution. The criteria like the maximum time termination [6] and termination-on convergence criteria [10] are also used as stopping criteria for the search process. The termination-on-convergence criteria is expressed by Lin and Miller [10] as.
fkx−fk−Γxfk−Γx<δE3
where δ is the ratio of the change in the objective function value, Γ = ηM, and η is the fraction of the maximum iterations (M) by which the change in the objective function is compared. As per this stopping criterion, if the enhancement over Γ generations is no longer than a threshold (δ), continuation of further iterations can be ineffective, and the search should be discontinued.
1.3 TS implementation procedure
The flow chart of TS algorithm is shown in Figure 1. Tabu Search begins with an initial solution xo. The neighbor solutions are created by altering the existing solution through a sequence of moves. The best new neighbor, x*, is used as the starting point for the next iteration, unless it is in the tabu list. Thus, even if no neighbor solutions are better than the starting solution, the best solution is still selected as the starting point for the next iteration. A record of the best solutions ever found, x*, is separately maintained. Also, the adaptive memory in tabu lists guides the search by utilizing the benefit of past information. This memory facilitates TS to make strategic choices and accomplish responsive exploration.
Figure 1.
Flow chart of the TS algorithm.
TS is implemented using the following steps.
Starts with an initial solution xo
Find the best solution, x* and define tabu list
Neighbor’s generations and neighborhood search
Define a neighborhood structure with respect to the solution space
Change the present solution to form a neighborhood of possible solutions
TS explore neighbor solution at each iteration
Searches entire neighborhood and select enhanced solution
Tabu list
Majority of the recent solutions are in tabu list
Older solutions are discarded
Short-term memory and long-term memory
Recency-based short-term memory (RSM)
Frequency-based long-term memory (FRM)
Intensification and Diversification
To search potential areas
To search whole feasible region
Aspiration criterion
To explore unvisited solutions
To evade feasible missing solutions
Stopping criteria
According iterations
Stopping on convergence
2. Application of Tabu search for optimal control of a polymerization reactor
The determination of open-loop time varying control policies that maximize or minimize a given performance index is referred as optimal control. The optimal control policies that guarantee the product property requirements and the operational constraints can be computed off-line, and are executed on-line in such a way that the process is operated in accordance with these control policies. Achievement of product quality is a major issue in polymerization processes since the molecular or morphological properties of a polymer product majorly influences its physical, chemical, thermal, rheological and mechanical properties as well as polymer applications. In a free radical copolymerization, composition drifts caused by variations in reactivities of comonomers can be mitigated by continuous addition of more reactive monomer while maintaining a constant mole ratio. The end use properties of the polymer product such as flexibility, strength and glass transition temperature are affected by the copolymer composition. Further, the molecular weight (MW) and molecular weight distribution (MWD) affects the important end use properties such as viscosity, elasticity, strength, toughness and solvent resistance. Hence, the determination of optimal control trajectories is important for the operation of polymerization reactors in order to produce a polymer with the desired product characteristics.
In the past, various methods have been reported for optimal control of polymerization reactors [12, 13, 14, 15, 16]. Most of the studies are based on classical methods of optimization such as Pontryagin’s maximum principle [17], which has been applied to solve the optimal control problems of different polymerization reactors [18, 19, 20, 21, 22, 23]. However, the classical methods have certain limitations for optimal control of polymerization reactors and these drawbacks have been discussed in literature [24]. The stochastic and evolutionary optimization methods are found beneficial over the conventional gradient-based search techniques because of their ability in locating the global optimum of multi-modal functions and searching design spaces with disjoint feasible regions.
2.1 Optimal control problem
The general open-loop optimal control problem of a lumped parameter batch/semi-batch process with fixed terminal time can be stated as follows. Find a control vector u(t) over tf [to, tf] to maximize (minimize) a performance index J(x,u):
Jxu=∫t0tfφxtuttdtE4
Subject to
ẋt=fxtutt,xt0=x0E5
hxtut=0E6
gxtut≤0E7
xL≤xt≤xUE8
uL≤ut≤uUE9
In the above, J refers the performance index, x is the state variable vector, u is the control variable vector. Eq. (5) represents the system of ordinary differential equations with their initial conditions, Eqs. (6) and (7) specify the equality and inequality algebraic constraints and Eqs. (8) and (9) are the upper and lower bounds for the state and control variables.
2.2 Multistage dynamic optimization strategy
A multistage optimization results due to the natural extension of a single stage optimization. In a system involving multiple stages, the output from one stage becomes the input to the subsequent stage. The multistage dynamic optimization procedure can be referred elsewhere [24]. This type of optimization needs special techniques to split the problem into computationally manageable units. In multistage dynamic optimization, the optimal control problem of the entire batch duration is divided into finite number of time instants referred to as discrete stages. The control variables and the corresponding state variables that satisfy the objective function are evaluated in stage wise manner.
In this work, a multistage dynamic optimization strategy with sequential implementation procedure is presented for optimal control of polymerization reactors. The procedure for solving the optimal control problem is similar to that of the dynamic programming based on the principle of optimality [25]. The meta heuristic features of tabu search (TS) are exploited by implementing this strategy on a semi-batch styrene–acrylonitrile (SAN) copolymerization reactor. The procedure involves in discretizing the process into N stages, defining the objective function, f i, the control vector, ui and the state vector, xi for stage i. This procedure is briefed in the following steps:
1. The optimum value of the objective function, f1[x1] for stage 1 driven by the best control vector u1 along with the state vector x1 is represented as
f1x1=minfo1x1u1u1E10
2. The value of the objective function, f2[x2] for stage 2 is determined based on the best control vector u2 along with the state vector x2 as given by
f2x2=f1x1+minfo2x2u2u2E11
3. Recursive generalization of the above procedure for the kth stage is represented by
fkxk=fk−1xk−1+minfokxkukukE12
In this procedure, fok represents the performance index of stage k.
2.3 The description of polymerization process and its mathematical representation
The solution copolymerization of styrene and acrylonitrile taking place in a semi-batch reactor is considered as a test bed for sequential implementation of the dynamic optimization strategy. The xylene is the solvent and AIBN is the initiator for the reaction. The feed which is a mixture of monomers, solvent, and initiator enters the reactor in semi-batch mode. The reactor initial volume is 1.01 L. The initially set design parameters are the solvent mole fraction fs = 0.25 and initiator concentration I0 = 0.05 mol/L. The mole ratio of monomers in the feed, M1/M2, is 1.5, where M1 and M2 are the molar concentrations of the unreacted monomers (styrene and acrylonitrile). The homogeneous solution free-radical copolymerization of styrene with acrylonitrile is described by the following reaction mechanism [26].
Initiation:
I→2R
R+M1→ki1P10E13
R+M2→ki2Q01
Propagation:
Pn,m+M1→kp11Pn+1,m
Pn,m+M2→kp12Qn,m+1E14
Qn,m+M1→kp21Pn+1,m
Qn,m+M2→kp22Qn,m+1
Combination termination:
Pn,m+Pr,q→ktc11Mn+r,m+q
Pn,m+Qr,q→ktc12Mn+r,m+qE15
Qn,m+Qr,q→ktc22Mn+r,m+q
Disproportionation termination:
Pn,m+Pr,q→ktd11Mn,m+Mr,q
Pn,m+Qr,q→ktd12Mn,m+Mr,qE16
Qn,m+Qr,q→ktd22Mn,m+Mr,q
Chain Transfer:
Pn,m+M1→kf11Mn,m+P10
Pn,m+M2→kf12Mn,m+Q01
Qn,m+M1→kf21Mn,m+P10E17
Qn,m+M2→kf22Mn,m+Q01
where Pn,m stand for a growing polymer chain with n units of monomer 1 (styrene) and m units of monomer 2 (acrylonitrile) with monomer 1 on the chain end. Similarly, Qn,m refers to a growing copolymer chain with monomer 2 on the end. The Mn,m denotes inactive or dead polymer.
The molecular weight (MW) and molecular weight distribution (MWD) of the copolymer are computed using three leading moments of the total number average copolymers. The instantaneous kth moment is given by:
λkd=∑n=1∞∑m=1∞nw1+mw2kMn,m,k=0,1,2,.……E18
where w1 is the molecular weight of styrene and w2 is the molecular weights of acrylonitrile. The total number average chain length (Xn), the total weight average chain length (Xw) and the polydispersity index (PD) are defined as:
Xn=λ1d/λ0d
Xw=λ2d/λ1dE19
PD=Xw/Xn
More details on modeling equations, reaction kinetics and numerical data pertaining to this system can be referred elsewhere [24].
The polymerization process model [24] is in the form of the general expression in Eq. (5). The set of state variables, X and the control vector U in the model are given by.
Xt=M1tM2tItVtλ0tλ1tλ2tT
and
Ut=TtutTE20
In the above, I is the concentration of the unreacted initiator, V is the reaction mixture volume, λk (k = 0, 1, …) is the kth moment of the dead copolymer molecular weight distribution, T is the reaction mixture temperature, an u is the volumetric flow rate of the feed mixture to the reactor.
2.4 Control objectives
The desired values of copolymer composition (F1D) and number average molecular weight (MWD) are chosen to be 0.58 and 30000, respectively. Minimizing the deviations of copolymer composition, F1 and molecular weight, MW from their respective desired values during the entire span of the reaction are specified as the desired objectives. In order to attain these objectives, the control variables are set as monomer addition rate, u and reactor temperature, T. If one manipulative variable is used to control one polymer quality parameter, the uncontrolled property parameters may deviate from their desired values as the reaction proceeds. The optimal control problem involves in optimizing the single objectives as well as both the objectives simultaneously. The objectives of SAN copolymerization are specified as.
J1=1−MWt/MWD2E21
J2=1−F1t/F1D2E22
J3=1−F1t/F1D2+1−MWt/MWD2E23
Here MW and F1 are the molecular weight and copolymer composition, and MWD and F1D are their respective desired values. The notation t here refers discrete time. The hard constraints are set as.
0≤ut≤0.07l/min
320≤Tt≤368kE24
Vt≤4.0l
These constraints on operating variables are selected by taking into consideration of reaction rate, heat transfer limitation and reactor safety. Determination of temperature policy, T, to satisfy J1 (Eq. (21)) and monomer feed policy, u, to satisfy J2 (Eq. (22)) are considered as single objective optimization problems. Determination of both u and T policies that satisfy J3 (Eq. (23)) is considered as a problem of simultaneous optimization.
2.5 Design and implementation
The design and implementation of tabu search for optimal control of copolymerization reactor is explained as follows. The total span of reaction time in SAN copolymerization reactor is split into finite number of time instants referred to discrete stages. The total time of reaction is fixed at 300 min. The duration of reaction time is divided into 19 stages with 20 time points, each stage having a duration of 15 min. Thus the discrete control sequences of feed flow rate, u and temperature, T are specified as.
u=u1u2..…u20TE25
T=T1T2..…T20TE26
The control sequences are located at equal distances. Initially, the control vector is specified as constant value at each of the discrete stages. The control input at the beginning of the first stage is chosen as the lower bound of the input space. The elements of tabu search for computing the optimal control policies are specified as follows. The sizes of both recency and frequency based tabu lists are set as 50. The sizes of these lists are chosen such that they prohibit revisiting of un-prosperous solutions in the search process. An intensification procedure in the form of a sine function is used. The oscillation period α of the sine function is controlled by a parameter (θ) whose value is 4.0001. A sigmoid function based aspiration criterion with the parameters as kcenter = 0.3 and σ = 7/M with M as specified number of iterations is used. For optimizing MW, ten neighbors are formed at the end of the first stage by considering random changes in the search space of T with an incremental change of −0.4 to 0.4. The number of neighbors specified for each control input of each stage is 10. The integration of process model is performed for a time period of 15 min with a time step of 1 min from the starting to the end of the first stage and the objective function values are calculated for all the generated neighbors at the end of this stage. The iterative convergence of TS leads to establish the best control input (T) along with its objective function. This provides the optimal control point for the first stage, which is then used as a starting point for the second stage solution. For second stage solution, random neighbors are created at the end of the second stage around the optimal T of the first stage. The integration of the model is performed from the beginning to the end of the first stage based on the initial control point (T) and from the starting to the end of the second stage for each of the neighbors generated at the end of second stage. The optimal control inputs for successive stages are computed until the end of last stage in a similar manner. The control input values that are computed at the end of each stage thus represents the optimal control policy for T. For F1 optimization, ten neighbors are generated at the end of first stage with an incremental variation of −1.0 x 10−6 to 1.0 x 10−6. In analogous manner, optimal control policy for u(F1) is found by following the similar TS procedure as in T policy. For determining the dual control policies of T and u, multistage dynamic optimization by TS is performed by accounting incremental variations in neighbors generation of T and u within the ranges of −0.4 to 0.4, and − 1.0 x 10−6 to 1.0 x 10−6, respectively. This case of multistage dynamic optimization involves the computation of the objective function values for 100 neighbor combinations at each of the control point corresponding to T and u.Figure 2 shows the implementation of TS strategy for optimal control of SAN copolymerization reactor.
Figure 2.
Multistage dynamic optimization of copolymerization reactor using tabu search.
2.6 Analysis of results
Tabu search (TS) is designed and applied to compute the optimal control policies that meet the single and multiple objectives of SAN copolymerization reactor. The dual control policies of T and u computed by TS for multistage dynamic optimization of polymerization reactor along with the objective function values are shown in Figure 3. These results exhibit the efficiency of TS in computing both the temperature and feed rate policies for the reactor to maintain MW and F1 almost near to their desired values. The computational efficiencies of TS are evaluated by means of execution times, normalized absolute error values and memory storage requirements as shown in Table 1.
Figure 3.
Dual control policies and objectives: (a) Temperature policy, (b) Feed rate policy, (c) Molecular weight as an objective, and (d) Copolymer composition as an objective.
Strategy
Control Policy
Computational efficiency
Normalized absolute error
Memory storage, k
Convergence time (sec)
Implementation time (sec)
TS
T
1.89
16.83
0.000566
2224
U
2.19
13.81
0.01379
2076
T & u
4.25
19.21
0.007535
3084
Table 1.
Computational efficiencies of TS strategy.
3. Application of Tabu search for inverse modeling of anaerobic fixed bed biofilm reactor
Tabu search is applied to determine the parameters of kinetic and film thickness models through the validation of the mathematical models of the process with the help of measured data acquired from an experimental fixed bed anaerobic biofilm reactor used in the treatment of pharmaceutical industry wastewater.
3.1 Experimental biofilm reactor and its description
The schematic of a laboratory scale fixed bed biofilm reactor setup used for industry waste water treatment is shown in Figure 4. The description of the experimental unit, its auxiliary items and the packing specifications are given as follows.
Figure 4.
Experimental biofilm reactor setup.
The reactor consists of a QVF glass column of 1 m height and 0.1016 m internal diameter. A Teflon perforated plate of thickness 3 mm is provided at the base of the column to support the packing material. Two openings fitted with valves made of Teflon are provided at the bottom of the reactor so that one valve is used to control the flow rate of influent pumped into the reactor and the other valve is used to discharge the excess sludge accumulated. The top of the column has a provision to place a thermometer to measure the temperature. Three sampling ports are placed at equal distances along the side of the column to withdraw samples. The temperature of the column is maintained by varying the voltage through the 0.2 kW heating tape connected to a dimmer-stat. The column is insulated with 1.0 in. asbestos rope. The entire setup is supported by a 1.0 in. M.S. pipeline structure. The column and the packing specifications are given elsewhere [27].
3.2 Experiments and data generation
The experimental setup shown in Figure 4 is used to conduct experiments for anaerobic treatment of pharmaceutical industry wastewater involving different packing materials with varying organic loading rates and feed rates, and different hydraulic retention times. The influent kept in a 2 l capacity vessel is fed to the column through an inlet connection located at the bottom using a peristaltic pump made of Watson Marlow. The effluent sample is collected from an outlet located at the top of the column. The column and the packing specifications are given elsewhere [27]. The reactor is filled with the packing material and then seeded with 1.0 l of active anaerobic sludge brought from M/s. Alkabir, Hyderabad, India. To maintain the initial growth of microorganisms, the reactor is further added with 2.6 l of very dilute solution of synthetic glucose medium (1000 mg/l) with nutrients such as total nitrogen as urea (125 mg/l), total phosphorous as KH2PO4 (50 mg/l), NaCl (50 mg/l), KCl (40 mg/l), CaCl2 (15 mg/l), MgCl2 (10 mg/l) and FeCl3 (2 mg/l). The pH of the solution is maintained at 7.2 by adding 0.1 N NaOH. The reactor is made biologically active by keeping it undisturbed for about 20 days. The gas (CH4 + CO2) evolved at the top of the column confirms the biological activity of microorganisms.
The wastewater procured from a typical pharmaceutical industry is a complex medium and its composition is reported elsewhere [28]. Substrates of varying COD concentrations are prepared using the wastewater in order to use them as feed solutions for biofilm reactor experiments. Once the biological activity of the bed is detected, the diluted industry wastewater solution equivalent to three bed volumes is sent to the reactor by an electronic dosing pump. NaHCO3 is added to maintain the pH of the feeding solution at 7.2. Different experiments are conducted for treating the pharmaceutical industry wastewater using the feed solutions having the COD concentrations of 4,980 mg/l, 11,860 mg/l, 23,460 mg/l and 40,720 mg/l. The hydraulic retention time (HRT) of each experiment is varied from 2 to 12 days based on the substrate concentration of the feed solution. Each experimental run subsequent to attainment of its HRT is allowed to continue for 13 days so as the operation reaches stable state condition by that time.
Thirteen experiments are conducted using the different feed solutions prepared from the pharmaceutical industry wastewater. The reactor is provided with the sampling ports to withdraw samples at bed heights of 0.25 m, 0.5 m and 0.75 m from the bottom. Samples collected from the three sampling ports of the column as well as from the effluent water are analyzed for COD, BOD, TVA, TA, pH etc. The stable state condition of each experiment is observed with respect to the minimal variation in reactor effluent pH, alkalinity and COD concentrations. Thus 13 experiments are conducted under different feed stream conditions. The data corresponding to the influent and effluent COD concentrations, HRT and OLR of all experiments are given elsewhere [28].
3.3 Mathematical and kinetic models
The application of mathematical models to biofilm reactors suffers due to lack of availability accurate kinetic models and uncertainty in model parameters. Therefore, appropriate selection of kinetic model and accurate determination of its parameters is required for successful modeling of biofilm reactors. The biological reaction rates are generally represented by Monod kinetics and also occasionally by Contois and Haldane models. In the past, efforts have been made to determine the parameters of kinetic models of biofilm reactors, mostly experimentally [29, 30, 31]. Various researchers [32, 33, 34, 35] have reported that numerical evaluation of kinetic parameters is an attractive alternative to the experimental methods for biofilm processes. By numerical approach, the parameters of the kinetic models of biofilm processes are determined as a consequence of the validation of their mathematical models with the aid of measured data. The approach of determining the model parameters such that the behavior of the process model approximates the observed process behavior is known as inverse modeling.
3.3.1 Mathematical models
Mathematical models of varying complexities involving different types of kinetic and film thickness models are used to represent the wastewater treatment process in the biofilm reactor.
3.3.1.1 One dimensional model
This model accounts the rate of mass transfer to be proportional to the concentration difference between the interface and the bulk fluid. This model assumes no accumulation of the component at the interface under steady state condition. The differential equation governing the fluid phase is given by.
−udcdz=kgavc−cssE27
with the boundary condition:
c=c0atz=0E28
In this model, the substrate concentration in the bulk fluid varies only in the axial direction.
The differential equation governing the solid phase is given by.
Dfξa−1ddξξa−1dcsdξ−rscs=0E29
with the boundary conditions:
dcsdξ=0atξ=0
kgcss−c=−Dfdcsdξatξ=LfE30
The superscript ‘a’ in Eq. (29) refers to 1, 2, and 3 for planar, cylindrical and spherical geometries, respectively, and Df denotes substrate diffusion coefficient in the biofilm (m2/day). The notation for other terms in the above equations is denoted as kg is mass transfer coefficient (m/s), av is specific surface area of particle (m−1), c is substrate concentration in the bulk fluid (kg/m3), cs is substrate concentration in the bio-film (kg/m3), css is substrate concentration on the bio-film surface (kg/m3), ξ is space coordinate in the bio-film (m), z is axial coordinate (m) and Lf is thickness of the bio-film (m).
3.3.1.2 Two dimensional model
This model considers the variation of the substrate concentration in bulk fluid in both the axial and radial directions. The substrate transfer occurring through the biofilm is characterized by physical diffusion and reaction, and this process is described by second order differential equation. Pressure losses along the length of the reactor are neglected. The differential equation governing the bulk fluid phase is given by.
udcdz=εDr∂∂rr∂c∂r−kgavc−cssE31
where D is substrate diffusion coefficient in the bulk fluid (m2/day), u is superficial velocity (m/s), r is radial coordinate (m) and ε is porosity of bed. The boundary condition for solving this equation is given in Eq. (28). The solid phase biofilm model for two dimensional model is same as in one dimensional model as in Eq. (29) and its boundary conditions are expressed by Eq. (30).
3.3.1.3 Mass transfer coefficient
The substrate mass transport occurring from the bulk fluid to the biofilm surface across the diffusion layer is defined by
jD=kgsc2/3uE32
where Sc is Schmidt number (μ/ρD). The jD-factor is calculated using the following correlation:
jDε=0.765Re0.82+0.365Re0.386E33
whereRe=ρudpμfor0.01<Re<15,000
where dp is equivalent particle diameter (m). The mass transfer coefficient, kg obtained from Eq. (32) is used in bulk fluid phase equations, Eq. (27) and Eq. (31).
3.3.2 Kinetic models
Various kinetic models can be used to represent the bioprocess kinetics [28], of which the Haldane and Edward models are given as follows.
3.3.2.1 Haldane model
This rate expression is generally valid when the substrate concentration is high. According to this model, the substrate consumption rate, rs in biofilm is given by the following equation:
rs=μmaxρs/YCsKs+Cs+Cs2KIE34
where Cs is substrate concentration, μmax is maximum specific growth rate, ρs is density of biomass, Y is yield coefficient, Ks is half velocity constant, and KI substrate inhibition constant.
3.3.2.2 Edward model
This model considers substrate inhibition, according to which the substrate consumption rate, rs in biofilm is given by the equation:
rs=μmaxρsYexp−CsKI−exp−CsKsE35
3.3.2.3 Film thickness
The biofilm thickness (Lf) is has significant influence on substrate conversion. A uniform film thickness with fixed value cannot represent the realistic situation and the film thickness Lf is expected to vary along the reactor [35]. The varying thickness of the biofilm is determined by the substrate flux from the bulk fluid into the biofilm as wellas the growth and decay rates of the bacteria. It is assumed that the biofilm is composed of a static portion and a variable portion. The variable portion is supposed to raise with the organic loading rate and lessen with the hydraulic loading rate. The above point of view leads to the following relations for estimating the biofilm thickness:
Lf=a+bOLRE36
Lf=a+bOLR−cHLRE37
where OLR is organic loading rate (kg/m3/day), HLR hydraulic loading rate (m/day), and a, b and c are constants to be determined.
3.4 Procedure for solving the model equations
To facilitate the solution of mathematical models, the height of the column (1 m) is divided into 50 equal steps, each step representing 0.02 m. In one dimensional model, the fluid phase equation (Eq. (27)) along with its boundary condition (Eq. (28)) is solved for each height step in the axial direction by using Runge–Kutta (RK) 4th order method. The solid phase equation for the biofilm (Eq. (29)) is solved for each segment using orthogonal collocation on finite elements (OCFE) [36]. Two finite elements, each with four internal collocation points are considered for OCFE implementation. In two dimensional model, the fluid phase equation (Eq. (31)) is transformed to ODE by finite difference technique and the resulting equation along with its boundary condition is solved by using 4th order RK method for each height step of the axial direction. The solution for solid phase equation of this model is same as in one dimensional model.
3.5 Tabu search for inverse modeling of biofilm reactor
The implementation procedure of tabu search is given in Section 1.3. In this work, tabu search is used to determine the parameters of kinetic and film thickness models in association with the validation of the mathematical models using the data of measurements obtained from an experimental fixed bed anaerobic biofilm reactor. The parameter estimation via inverse modeling is carried out by defining an objective function, J given by.
J=fα=∑i=1lyi−ŷi2E38
where α is the vector of parameters, l is the number of observations, yi is the measured value of the ith variable, and ŷi is the corresponding predicted value. Tabu search is applied to estimate the parameters of kinetic and film thickness expressions of different modeling configurations with the support of one dimensional (1D) and two dimensional (2D) mathematical models of the biofilm reactor. Random variation in all the parameters is considered to generate neighbors so as to provide the maximum improvement to the current solution. Recency based tabu list with a length of 100 and frequency based tabu list with a length of 50 are employed. A sigmoid function based aspiration criterion, Eq. (2) is employed with kcenter as 0.3 and σ as 7/M, where M refers specified number of iterations. An intensification strategy with the coefficient α taking the format of a sine function, Eq. (1) is employed, in which the value of θ is assigned to be 4.0001. The maximum number of iterations are considered as 100. The termination-on-convergence criteria, Eq. (3) is used as stopping criterion.
3.6 Analysis of results
Parameter estimation by tabu search is performed by devising different modeling configurations to represent the biofilm reactor. These configurations involve the Edward kinetics and Haldane kinetics with substrate inhibition along with the two and three parameter film thickness expressions. The modeling configuration that is formed by 1D model along with Haldane kinetics and two parameter film thickness expression is referred to 1D-Haldane-2film. Other modeling configurations are formed and abbreviated in the same manner. The effectiveness of these modeling configurations are assessed by comparing the model predictions with experimental data and further by means of performance measures such as cost function (CF) and model efficiency (ME) [28]. A conventional optimization method called Nelder–Mead optimization (NMO) [37, 38] is also employed for comparison with the tabu search. The results are analyzed to find the better suitability of mathematical models using the quantitative performance measures (CF and ME). These results evaluated for 1D and 2D models with Haldane and Edward kinetics involving two film and three film expressions indicate the better suitability of 2D model over 1D model. When the results are analyzed to assess the better suitability optimization algorithm, the analysis of results of different modeling configurations indicate the effectiveness of TS over NMO. The results evaluated to find the usefulness of kinetic models indicate the better suitability of Edward kinetics over Haldane kinetics. The results analyzed to assess the film thickness expressions indicate the appropriateness of the three parameter film thickness expression over two parameter expression. The iterative convergence of parameters estimated by TS and NMO are shown in Figure 5. The comparison of the prediction results of 2D model with Edward kinetics and three parameter film thickness expression evaluated using TS and NMO with those of experimental results are shown in Figure 6. The analysis of the results show the better performance of TS over NMO for inverse modeling of biofilm reactor. From these results, it is found that the TS involving 2D model, Edward kinetics and three parameter film thickness expression better represents the fixed bed biofilm reactor involved in the treatment of pharmaceutical industry wastewater.
Figure 5.
Iterative convergence of parameter estimates by TS and NMO: (a) kinetic parameters, (b) film thickness parameters.
Figure 6.
Comparison of experimental results with model predicted substrate conversions of 2D model with Edward kinetics.
4. Conclusions
Tabu search is a stochastic optimization method used to solve global optimization problems. The effectiveness of tabu search for modeling and optimization is explored with the applications concerning to chemical and environmental systems of varying complexities. The meta heuristic Tabu search (TS) is designed and applied to determine the optimal control policies of a SAN copolymerization reactor and inverse modeling of a biofilm reactor. The computational efficiencies of TS are evaluated in terms of execution times, normalized absolute error values and memory storage requirements. The results of polymerization reactor show the usefulness of TS in determining the optimal temperature and feed rate policies to maintain the objectives MW and F1 near to their desired values. The results of biofilm reactor explain the efficacy of TS in appropriately configuring the kinetic and film thickness models as a consequence of validation of mathematical models.
\n',keywords:"Tabu search, Metaheuristic approach, Adaptive memory, Copolymerization reactor, Biofilm reactor",chapterPDFUrl:"https://cdn.intechopen.com/pdfs/77046.pdf",chapterXML:"https://mts.intechopen.com/source/xml/77046.xml",downloadPdfUrl:"/chapter/pdf-download/77046",previewPdfUrl:"/chapter/pdf-preview/77046",totalDownloads:46,totalViews:0,totalCrossrefCites:1,dateSubmitted:"November 27th 2020",dateReviewed:"May 4th 2021",datePrePublished:"June 4th 2021",datePublished:null,dateFinished:"June 4th 2021",readingETA:"0",abstract:"Stochastic optimization methods are increasingly used for optimizing processes that are difficult to solve by conventional techniques. These methods are widely employed to optimize the processes which have higher dimensionality with severe nonlinearities. Different methods of this kind include the genetic algorithm (GA), simulated annealing (SA), differential evolution (DE), ant colony optimization (ACO), tabu search (TS), particle swarm optimization (PSO), artificial bee colony (ABC) algorithm, and cuckoo search (CS) algorithm. Among these methods, tabu search (TS) is a potential tool used to find a feasible optimal solution from a finite set of solutions. The memory used in TS will remember the current best solution and it also enables the TS to track the last solutions while guiding the search moves. The capability of memory and strategic adaptation features of TS enable it to make use of good solutions and also search for new feasible regions in the search space. TS has been successfully applied to solve a wide spectrum of optimization problems in different disciplines. This chapter describes the TS algorithm in detail and its applications to chemical and environmental processes, specifically, dynamic optimization of a copolymerization reactor and inverse modeling of a biofilm reactor. In dynamic optimization of copolymerization reactor, the meta heuristic Tabu search (TS) is designed and applied to determine the optimal control policies of a styrene–acrylonitrile (SAN) copolymerization reactor. In inverse modeling of biofilm reactor, the tabu search is designed and applied to determine the parameters of kinetic and film thickness models as consequence of the validation of the mathematical models of the process with the aid of measured data acquired from an experimental fixed bed anaerobic biofilm reactor used in the treatment of pharmaceutical industry wastewater. For both the cases, optimization by Tabu search is carried out by suitably formulating the desired objective functions and the problems are solved by encoding the variables and parameters using real floating point numbers. The results explain the efficacy of TS for optimal control of polymerization reactor and inverse modeling of biofilm reactor.",reviewType:"peer-reviewed",bibtexUrl:"/chapter/bibtex/77046",risUrl:"/chapter/ris/77046",signatures:"Chimmiri Venkateswarlu",book:{id:"10627",type:"book",title:"Engineering Problems - Uncertainties, Constraints and Optimization Techniques",subtitle:null,fullTitle:"Engineering Problems - Uncertainties, Constraints and Optimization Techniques",slug:null,publishedDate:null,bookSignature:"Dr. Marcos Sales Guerra Tsuzuki and Prof. Rehab O. Abdel Rahman",coverURL:"https://cdn.intechopen.com/books/images_new/10627.jpg",licenceType:"CC BY 3.0",editedByType:null,isbn:"978-1-83969-368-7",printIsbn:"978-1-83969-367-0",pdfIsbn:"978-1-83969-369-4",isAvailableForWebshopOrdering:!0,editors:[{id:"146384",title:"Dr.",name:"Marcos Sales Guerra",middleName:null,surname:"Tsuzuki",slug:"marcos-sales-guerra-tsuzuki",fullName:"Marcos Sales Guerra Tsuzuki"}],productType:{id:"1",title:"Edited Volume",chapterContentType:"chapter",authoredCaption:"Edited by"}},authors:null,sections:[{id:"sec_1",title:"1. Introduction",level:"1"},{id:"sec_1_2",title:"1.1 Basic principle",level:"2"},{id:"sec_2_2",title:"1.2 Components of TS",level:"2"},{id:"sec_2_3",title:"1.2.1 Neighbors generations and neighborhood search",level:"3"},{id:"sec_3_3",title:"1.2.2 Tabu list",level:"3"},{id:"sec_4_3",title:"1.2.3 Short-term memory and long-term memory",level:"3"},{id:"sec_5_3",title:"1.2.4 Intensification and diversification",level:"3"},{id:"sec_6_3",title:"1.2.5 Aspiration criterion",level:"3"},{id:"sec_7_3",title:"1.2.6 Stopping criteria",level:"3"},{id:"sec_9_2",title:"1.3 TS implementation procedure",level:"2"},{id:"sec_11",title:"2. Application of Tabu search for optimal control of a polymerization reactor",level:"1"},{id:"sec_11_2",title:"2.1 Optimal control problem",level:"2"},{id:"sec_12_2",title:"2.2 Multistage dynamic optimization strategy",level:"2"},{id:"sec_13_2",title:"2.3 The description of polymerization process and its mathematical representation",level:"2"},{id:"sec_14_2",title:"2.4 Control objectives",level:"2"},{id:"sec_15_2",title:"2.5 Design and implementation",level:"2"},{id:"sec_16_2",title:"2.6 Analysis of results",level:"2"},{id:"sec_18",title:"3. Application of Tabu search for inverse modeling of anaerobic fixed bed biofilm reactor",level:"1"},{id:"sec_18_2",title:"3.1 Experimental biofilm reactor and its description",level:"2"},{id:"sec_19_2",title:"3.2 Experiments and data generation",level:"2"},{id:"sec_20_2",title:"3.3 Mathematical and kinetic models",level:"2"},{id:"sec_20_3",title:"3.3.1 Mathematical models",level:"3"},{id:"sec_20_4",title:"3.3.1.1 One dimensional model",level:"4"},{id:"sec_21_4",title:"3.3.1.2 Two dimensional model",level:"4"},{id:"sec_22_4",title:"3.3.1.3 Mass transfer coefficient",level:"4"},{id:"sec_24_3",title:"3.3.2 Kinetic models",level:"3"},{id:"sec_24_4",title:"3.3.2.1 Haldane model",level:"4"},{id:"sec_25_4",title:"3.3.2.2 Edward model",level:"4"},{id:"sec_26_4",title:"3.3.2.3 Film thickness",level:"4"},{id:"sec_29_2",title:"3.4 Procedure for solving the model equations",level:"2"},{id:"sec_30_2",title:"3.5 Tabu search for inverse modeling of biofilm reactor",level:"2"},{id:"sec_31_2",title:"3.6 Analysis of results",level:"2"},{id:"sec_33",title:"4. 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Nonlinear Analysis in Chemical Engineering. McGraw-Hill Chemical Engineering Series. New York: McGraw-Hill; 1980'},{id:"B37",body:'Kuester JL, Mize JH. Optimization Techniques with Fortran. New York: McGraw-Hill; 1973'},{id:"B38",body:'Venkateswarlu C, Gangiah K. Dynamic modeling and optimal state estimation using extended kalman filter for a kraft pulping digester. Ind. Eng. Chem. Res. 1992;31:848-855'}],footnotes:[],contributors:[{corresp:"yes",contributorFullName:"Chimmiri Venkateswarlu",address:"chvenkat.iict@gmail.com",affiliation:'
Indian Institute of Chemical Technology (CSIR-IICT), Hyderabad, India
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Kang",authors:[{id:"144252",title:"Dr.",name:"Gurjaipal",surname:"Kang",fullName:"Gurjaipal Kang",slug:"gurjaipal-kang",email:"drpaulkang@gmail.com"},{id:"155147",title:"Mr.",name:"Kevin",surname:"Kang",fullName:"Kevin Kang",slug:"kevin-kang",email:"kevinsinghkang@gmail.com"}],book:{id:"2818",title:"Aneurysm",slug:"aneurysm",productType:{id:"1",title:"Edited Volume"}}}],collaborators:[{id:"46440",title:"Dr.",name:"Efstratios",surname:"Georgakarakos",slug:"efstratios-georgakarakos",fullName:"Efstratios Georgakarakos",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"Democritus University of Thrace",institutionURL:null,country:{name:"Greece"}}},{id:"142765",title:"Dr.",name:"Guillermo",surname:"Vilalta",slug:"guillermo-vilalta",fullName:"Guillermo Vilalta",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:null},{id:"142985",title:"PhD.",name:"Tomasz",surname:"Szmuda",slug:"tomasz-szmuda",fullName:"Tomasz Szmuda",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:null},{id:"143555",title:"Dr.",name:"Soh",surname:"Hosoba",slug:"soh-hosoba",fullName:"Soh Hosoba",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"Shiga University of Medical Science",institutionURL:null,country:{name:"Japan"}}},{id:"144252",title:"Dr.",name:"Gurjaipal",surname:"Kang",slug:"gurjaipal-kang",fullName:"Gurjaipal Kang",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:"CURRICULUM VITAE \n \n\n\nGurjaipal (Paul) Singh Kang MD FACC FACP FSCAI\n\nDOB: September 1, 1968\n\nCitizenship: United States\n\nAddress: 4368 Winners Circle \n\nErie, PA 16506\n\nTelephone: 814 833-4446\n\nFax No: 814 833-2281 \n\n\nEducation and Employment \n\n3/2007-Present: Director of Cardiac Catheterization Laboratory – Hamot\nMedical Center \n\n1/2003-Present: Director of Invasive Cardiac Services—Meadville\nMedical Center\n\n7/2001-Present: Hamot Medical Center : Intervention/Cardiovascular\nDisease\n\n7/2001-Present: Medicor Associates, Inc., 120 East Second Street,\nErie, PA 16507 \n\nPartner 7/2004\n\n7/2000-6/2001: Interventional Cardiology fellow at University\nHospitals of Cleveland/Case Western \n\nReserve University\n\n7/1999-6/2000: Assistant Professor of Medicine/Cardiology at Temple\nUniversity, Philadelphia. \n\nAttending Physician/Cardiologist at Temple University Hospital,\nPhiladelphia, PA. \n\n(Very active in cardiac catheterization, echocardiography, coronary care\nunit and \n\nclinical cardiology).\n\n7/1999-6/1999: Chief Fellow, Cardiovascular Diseases, Case Western\nReserve University/University \n\nHospitals of Cleveland.\n\n7/1997-6/1998: Fellow, Cardiovascular Diseases, Case Western Reserve\nUniversity/Univ. Hospitals of \n\nCleveland.\n\n7/1996-6/1997: Fellow, Cardiovascular Diseases, Mt. Sinai School of\nMedicine, Elmhurst Hospital \n\n Program.\n\n7/1995-6/1996: Chief Resident, Loma Linda University School of\nMedicine Internal Medicine \n\nResidency Program.\n\n7/1995-6/1996: Attending Physician Riverside General\nHospital/Instructor-Loma Linda University \n\nSchool of Medicine.\n\n7/1993-6/1995: Resident, Internal Medicine Loma Linda University\nMedical Center\n\n7/1992-6/1993: Resident, Internal Medicine Albert Einstein\nUniversity/Flushing Hospital Program\n\n8/1986-1/1992: Medical Student Government Medical College, Amritsar,\nPunjab, India\n\n6/1984-6/1986: Pre-Medical Student Khalsa College, Amritsar, Punjab,\nIndia.\n\n1/1973-4/1984: Student, St. Francis School, Amritsar, Punjab, India. \n\nBoard Certified In: \n\n2009: Board recertification in echocardiography 92%\n\n2009: Board certified in Endovascular and Vascular Medicine. ABVM\ndiplomat.\n\n2009: Recertification in Cardiovascular medicine boards – Decile 10 \n\n Recertification in Nuclear Cardiology and Interventional Cardiology\nexamination\n\n2007: Cardiac CT Level II Certificate \n\n2005: Re-certification-Internal Medicine Boards Decile 10\n\n2001: American Board of Internal Medicine: Interventional Cardiology\n\n1999: American Board of Internal Medicine: Examination Percentage:\nOverall 87%. Decile 10. EKG \n\ncomponent 89%: Cardiovascular Disease\n\n1999: Certification Board of Nuclear Cardiology. Percentage: Overall\n89%: Nuclear Cardiology. \n\nGurjaipal S. Kang, M.D.\n\nPage 2 \n\n\n1999: National Board of Echocardiography. Percentile 92% - Adult\nComprehensive Echocardiography.\n\n1995: American Board of Internal Medicine. Deciles 9 & 8: Internal\nMedicine.\n\n1995: Internal Medicine Intraining Examination. Percentile 97% plus.\n\n1992: FMGEMs examinations. Scores 87 & 85. \n\n\nResearch:\n\nPeer Reviewed Publications:\n\n2011: EuroIntervention Journal (European Association of Percutaneous Cardiovascular Interventions (EAPCI)) Abstract published on Excellent Femoral results with Perclose for oral presentation in EuroPCR 2011\n\n2007: American Journal of Emergency Medicine, SVG Aneurysm leading to\ntamponade- \n\nKang, G, et al.\n\n2006: American Journal of Emergency Medicine, Spontaneous Coronary\nDissection, Kang, G, et al.\n\n2006: Southern Medical Journal, Tamponade in Thyroid Disease, Ashvath\nM., Kang, G, et al.\n\n2005: American Journal of Geriatric Cardiology, New Diagnosis of Left\nAtrial Myxoma in a 93 Cardiology-Kang GS, Sanchez \n\nB, Kang MK, Hansen C: Effect of exercise induced hypertension on left\nventricular hypertrophy \n\nin normotensive individuals.\n\nPresentations in Major International Meetings:\nCRT 2012, Washington DC. Results in Femoral Artery practice with only board certified cardiologists doing the stick. Accepted for poster presentation.\nEuro PCR 2011, Paris France. Excellent results from Perclose technology compared to Radial approach ORAL PRESENTATION.\nICCAD 2009: Poster Presentation: International Congress of Coronary Artery Disease Prague Czech Republic. A very large perclose experience with no infections\nFortis Hospital International Global Conference 2011 Session Moderator. Guest Speaker.\n\n\n2000: Poster presentation-Pennsylvania Chapter of American College of\nCardiology-Kang GS, Zheng JS, Kang MK, Rothman S, Thames MD: Usefulness\nof D-Dimer testing in evaluation of left atrial\n\nthrombi.\n\n1995: International Heart Failure in Geneva, Switzerland-Engel G, Kang\nGS, Sweeney M et al: \n\nSignificant improvements in LV systolic function possible in patients\nattending a cardiomyopathy\n\nclinic.\n\n1995: Loma Linda University Annual Meeting Honoring Research-Engel G,\nKang GS, Sweeney M \n\net al: Significant improvements in systolic function possible in\npatients attending a cardiomyopathy clinic.\n\nCompleted abstracts pending submission:\n\n2000: Kang GS, Rothman S, Hansen C et al: Effect of exercise induced\nhypertension on left ventricular hypertrophy in\n\nnormotensive individuals.\n\n2000: Pending resubmission to American Association of Medical Colleges\n(RIME conference)- \n\nKang GS, Loo L, Bouland D: Improvement in documentation due to an\nintroduction of a peer \n\nreview conference in the residents’ monthly schedule.\n\nCompleted manuscripts pending submission:\n\n2000: CHEST journal-Kang GS, Farah MG: Early diagnosis of aortic abscess\nusing transesophageal \n\nechocardiography.\n\nResearch Awards:\n\n1995: Presenter of the winning abstract in Loma Linda University Annual\nMeeting Honoring Research- Engel G, Kang GS, Sweeney M et al:\nImprovements in LV systolic function possible in patients \n\nattending a cardiomyopathy clinic.\n\n1993: Certificate of Merit from Flushing Hospital Medical Center for a\nvery high number of patient \n\nenrollment in Digoxin Investigation group trial. \n \n\n\nGurjaipal S. Kang, M.D.\n\nPage 3 \n\n\nOther Research Experience:\n2011: Primary Investigator Dalcetrapib outcomes large randomized trial-multi center.\n\n2009-ongoing Sub-Investigator – Carotid Stenting for High Surgical\nRisk Patients; Evaluating Outcomes \n\nthrough the collection of Clinical Evidence (“CHOICE”)\n\n2009-ongoing Primary Investigator - APPRAISE-2 A Phase 3, Randomized,\nDouble-Blind, Evaluation \n\nof the Safety and Efficacy of Apixaban in Subjects with a Recent Acute\nCoronary \n\nSyndrome\n\n2009 Sub-Investigator – A Prospective, Randomized,\nMulti-Center, Double-Blind Trial to \n\nAssess the Effectiveness and Safety of Different Durations of Dual\nAnti-Platelet Therapy \n\n(DAPT) in Subjects Undergoing Percutaneous Coronary Intervention with\nthe ENDEAVOR \n\nZatoralimus-eluting Coronary Stent (CYPHER ® Stent)\n\n2009. Primary Investigator – The PROTECT Continued Access\nPost Marketing Surveillance \n\nTrial\n\n2008-ongoing Sub-Investigator-A Prospective, Non-Randomized, Two Arm\nMulti-Center Clinical Trial to Evaluate the \n\nSafety and Efficacy of the Absolute Pro ™ Peripheral Self-Expanding\nStent System and \n\nThe Omnilink Elite ™ Peripheral Balloon-Expandable Stent System in\nSubjects with \n\nAtherosclerotic DE NOVO or Restenotic Lesions in the Native Common Iliac\nArtery \n\nAnd/or Native External Iliac\n\n2008-Ongoing Principal Investigator-A Multi-center, Randomized,\nDouble-Blind, Placebo – Controlled Study to Evaluate the \n\n\nSafety and Efficacy of SCH530348 in addition to standard of care in\nsubjects with Acute \n\nCoronary Syndrome: Thrombin Receptor Antagonist for Clinical Event\nReduction in \n\nAcute Coronary Syndrome (TRA-CER)\n\n2009. Sub-Investigator-Variation in Recovery: Role of\nGender on Outcomes in Acute Myocardial Infarction \n\n(AMI) Patients (VIRGO)\n\n2008 Sub-Investigator – XIENCE V™ Everolimus Eluting\nCoronary Stent System (EECSS) \n\nEXCEED: Evaluation of XIENCE V™ for Catheterization Lab Endpoints a2009. Sub-Investigator – CAPTURE 2 A post-approval Study of\nthe Guidant acculink stent \n\nSystems and accunet embolic protection systems, Carotid RX ACCULINK/ to\nUncover \n\nUnanticipated and Rare Events\n\n2005-2006 Primary Investigator – The ACUITY Trial: A randomized\ncomparison of Angiomax ® \n\n(bivalirudin) versus heparin (unfractionated heparin or enoxaparin) in\npatients under \n\ngoing early invasive management for acute coronary syndromes without\nST-segment \n\nelevation\n\n2006. Primary Investigator – APEX – A Multicenter,\nRandomized, Double-Blind, Parallel- \n\nGroup, Placebo-Controlled Study of Pexelizumab in patients with Acute\nMyocardial\n\nInfarction undergoing Primary Percutaneious Coronary Intervention\n\n2000. Principal Investigator -Schering Plough Multicenter\ntrial- To evaluate the safety and \n\nEfficacy of SCH 58235: Phase III Double-Blind Efficacy and Safety study\nof a new \n\nAntilipid agent \n\nCollecting prospective data on Discomfort during cardiac catheterization\n(DOC) study\n\n1998. Obtained Institutional Review Board approval as the\nChief Investigator in a trial to \n\nEvaluate hemodynamics of Medtronic stentless valve in aortic position.\n\n1998. Applied for ACC/Merck fellowship award and AHA\naffiliate in training award for role \n\nOf impaired sensitivity of cardiopulmonary and aortic baroreceptors in\nrapid pacing \n\nInduced model of heart failure.\n\n1994. Evaluated role of E Wave to reverse E Wave transit\ntime in impaired relaxation in LVH. \n\n \n\n \n \n\n\nGurjaipal S. Kang, M.D.\n\nPage 4 \n\n\nInvited Lectures:\n\nCME accredited lectures: \n\n2000-2005: Multiple Cardiology Grand Rounds at Hamot Medical Center.\n\n1999: Scientific Exchange Incorporation (Connecticut) sponsored\nlectures on Clinical paradigms in \n\nmanagement of atherosclerosis: in Albany and Houston.\n\n1998-1999: Full series of lectures to cardiology faculty and fellows in\nCase Western Reserve University \n\nto cover topics of American Society of Echocardiography examination.\n\n1996-1998: Grand round presentations in Case Western Reserve\nUniversity/University Hospitals of \n\nCleveland. \n\nGrand Rounds in Elmhurst Hospital, NY.\n\n1998-1999: Presented an average of one lecture per week during the\nchief cardiology fellowship. \n\nSuperior evaluation by housestaff for conference presentations.\n\n1999-2000: Bristol Myers Squib and Merck sponsored lectures to\ncardiology and medicine house staff on\n\nhypercholesterolemia, inflammatory mediators of coronary artery disease,\nrole of ace- inhibitors \n\nand angiotensin receptor blockers in heart failure.\n\n1998: Lectures as a part of teaching curriculum of 2nd year medical\nstudents at Loma Linda University \n\nand Case Western Reserve University.\n\n1995-1996: An average of one lecture per week to medicine house staff\nand 3rd and 4th year medical \n\nstudents as Chief Resident at Loma Linda University. \n\n\nAwards and Honors:\n\n2011: Fortis Hospital India Global Conference award for Speaker/Session Moderator\n\n2009: TRACER trial award for very high enrollment in a randomized trial\n\n7/1998-6/1999: Chief Fellow in Cardiology-Case Western Reserve\nUniversity/University Hospitals of\n\nCleveland.\n\n7/1995-6/1996: Chief Resident in Internal Medicine-Loma Linda University\nInternal Medicine Program.\n\n1995: Presented the Winning abstract in the Loma Linda University Annual\nMeeting Honoring Research.\n\n1995: Scored above the national percentile scale, 97 percentile plus in\nNational Intraining Examination of the American Board of Internal\nMedicine.\n\n1994-1995: Awards for top scores in the core curriculum examinations\nin Loma Linda University\n\nResidency program.\n\n1995: Recipient of second highest votes for the outstanding resident of\nthe year from other residents and\n\nfaculty at Loma Linda University and three affiliated hospitals.\n\n1995: 90% score in Department of Health Services Examination,\nCalifornia.\n\n1986: Position 171986: Governor’s invitation for academic achievement in Punjab, India.\n\n1986: Placed in Khalsa College Merit List for academic achievements.\n\n1984: Gold Medal and First Position in ICSE (Indian Certificate of\nSecondary Education Examinations)\n\nFirst position in class from third grade up to graduation during high\nschool & elementary school\n\neducation. \n\n\nLicensure and Certification:\n\nLicensed in:\n\nPennsylvania: Expiration date 12/31/10\n\nOhio: Expiration date 10/01/10\n\nNew York: Expiration date 08/31/11\n\nCalifornia: Expiration date 09/30/11 \n\nGurjaipal (Paul)Singh Kang M.D\n\nPage 5 \n\n\nProfessional Fellowships:\n\nFellow of American College of Cardiology\n\nFellow of American College of Physicians\n\nFellow of Society of Coronary angiography and interventions.\n\n\n \n\n\nInterests and Hobbies:\n\nRunners up in Table Tennis in National Medical College Games in New\nDelhi, India, 1988\n\nCollege Colors (highest honors for sports achievement in Govt. Medical\nCollege), 1991\n\nMember of College soccer, table tennis and track teams. \n\nCommunity Work\n \n\n\n\nFree Vascular Screenings offered to public in the Erie, PA mall and\nother settings.",institutionString:null,institution:{name:"University of Pittsburgh",institutionURL:null,country:{name:"United States of America"}}},{id:"144628",title:"Prof.",name:"Ahmad Subhy",surname:"Alsheikhly",slug:"ahmad-subhy-alsheikhly",fullName:"Ahmad Subhy Alsheikhly",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/144628/images/2666_n.jpg",biography:"Professor of Emergency Surgery and Medicine at Hamad Medical corporation and Weill Cornell medical college-Qatar, he received his MB, CHB degree from Salahaddin medical college, north of Iraq at 1983, then became a qualified surgeon by getting the fellowship of Arab Board in General Surgery at 1994, that was followed by the FRCSI (Fellow of the Royal College of surgeons in Ireland) at 2004. Now he is a member of the European society of intensive care medicine (ESICM), the American college of emergency physicians (ACEP) and international society of surgery (MISS/SIC). He has published more than 32 studies including original, case report and review articles all over the world, in addition to a book in Human anatomy and a chapter of Splenic artery aneurysm in a book titled (Aneurysm) at 2012. He has been participating very actively in large groups of conferences as presenter, supervised post graduate candidates, as well as sharing his clinical work as emergency physician and surgeon, training undergraduate medical students, and leading many researchers to achieve and publish their studies.",institutionString:null,institution:{name:"Weill Cornell Medical College in Qatar",institutionURL:null,country:{name:"Qatar"}}},{id:"145482",title:"Prof.",name:"Pawel",surname:"Sloniewski",slug:"pawel-sloniewski",fullName:"Pawel Sloniewski",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:null},{id:"147938",title:"Dr.",name:"Yasuo",surname:"Murai",slug:"yasuo-murai",fullName:"Yasuo Murai",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/147938/images/system/147938.jpg",biography:"Dr. Yasuo Murai MD, PhD who graduated from Nippon Medical School in 1993, trained at the Department of Neurosurgery, Nippon Medical School and specialized in Neurovascular surgery and skull base surgery at the Nippon Medical School hospital. His areas of expertise include neurovascular surgery, vascular reconstructive surgery and skull base neurosurgery both within Japan and abroad. A highly respected surgeon, teacher and researcher, he is one of the leading authorities on advanced vascular reconstructive surgery in Japan. He is the author of many peer-reviewed articles on these topics. He has been serving as acting head of the Nippon Medical School of neurovascular surgery and is an internationally recognized authority in vascular reconstructive surgery. He is currently clinical Assistant Professor of the Department of Neurosurgery at the Nippon Medical School hospital. He has received numerous scientific awards for his contributions to neurovascular surgery within Japan",institutionString:null,institution:{name:"Nippon Medical School",institutionURL:null,country:{name:"Japan"}}},{id:"147939",title:"Prof.",name:"Akira",surname:"Teramoto",slug:"akira-teramoto",fullName:"Akira Teramoto",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"Nippon Medical School",institutionURL:null,country:{name:"Japan"}}},{id:"148452",title:"Prof.",name:"Tohru",surname:"Asai",slug:"tohru-asai",fullName:"Tohru Asai",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"Shiga University of Medical Science",institutionURL:null,country:{name:"Japan"}}}]},generic:{page:{slug:"open-access-funding-funders-list",title:"List of Funders by Country",intro:"
If your research is financed through any of the below-mentioned funders, please consult their Open Access policies or grant ‘terms and conditions’ to explore ways to cover your publication costs (also accessible by clicking on the link in their title).
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IMPORTANT: You must be a member or grantee of the listed funders in order to apply for their Open Access publication funds. Do not attempt to contact the funders if this is not the case.
",metaTitle:"List of Funders by Country",metaDescription:"If your research is financed through any of the below-mentioned funders, please consult their Open Access policies or grant ‘terms and conditions’ to explore ways to cover your publication costs (also accessible by clicking on the link in their title).",metaKeywords:null,canonicalURL:"/page/open-access-funding-funders-list",contentRaw:'[{"type":"htmlEditorComponent","content":"
UK Research and Innovation (former Research Councils UK (RCUK) - including AHRC, BBSRC, ESRC, EPSRC, MRC, NERC, STFC.) Processing charges for books/book chapters can be covered through RCUK block grants which are allocated to most universities in the UK, which then handle the OA publication funding requests. It is at the discretion of the university whether it will approve the request.)
UK Research and Innovation (former Research Councils UK (RCUK) - including AHRC, BBSRC, ESRC, EPSRC, MRC, NERC, STFC.) Processing charges for books/book chapters can be covered through RCUK block grants which are allocated to most universities in the UK, which then handle the OA publication funding requests. It is at the discretion of the university whether it will approve the request.)
Wellcome Trust (Funding available only to Wellcome-funded researchers/grantees)
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His studies in robotics lead him not only to a PhD degree but also inspired him to co-found and build the International Journal of Advanced Robotic Systems - world's first Open Access journal in the field of robotics.",institutionString:null,institution:{name:"TU Wien",country:{name:"Austria"}}},{id:"441",title:"Ph.D.",name:"Jaekyu",middleName:null,surname:"Park",slug:"jaekyu-park",fullName:"Jaekyu Park",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/441/images/1881_n.jpg",biography:null,institutionString:null,institution:{name:"LG Corporation (South Korea)",country:{name:"Korea, South"}}},{id:"465",title:"Dr.",name:"Christian",middleName:null,surname:"Martens",slug:"christian-martens",fullName:"Christian Martens",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"Rheinmetall (Germany)",country:{name:"Germany"}}},{id:"479",title:"Dr.",name:"Valentina",middleName:null,surname:"Colla",slug:"valentina-colla",fullName:"Valentina Colla",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/479/images/358_n.jpg",biography:null,institutionString:null,institution:{name:"Sant'Anna School of Advanced Studies",country:{name:"Italy"}}},{id:"494",title:"PhD",name:"Loris",middleName:null,surname:"Nanni",slug:"loris-nanni",fullName:"Loris Nanni",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/494/images/system/494.jpg",biography:"Loris Nanni received his Master Degree cum laude on June-2002 from the University of Bologna, and the April 26th 2006 he received his Ph.D. in Computer Engineering at DEIS, University of Bologna. On September, 29th 2006 he has won a post PhD fellowship from the university of Bologna (from October 2006 to October 2008), at the competitive examination he was ranked first in the industrial engineering area. He extensively served as referee for several international journals. He is author/coauthor of more than 100 research papers. He has been involved in some projects supported by MURST and European Community. His research interests include pattern recognition, bioinformatics, and biometric systems (fingerprint classification and recognition, signature verification, face recognition).",institutionString:null,institution:null},{id:"496",title:"Dr.",name:"Carlos",middleName:null,surname:"Leon",slug:"carlos-leon",fullName:"Carlos Leon",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"University of Seville",country:{name:"Spain"}}},{id:"512",title:"Dr.",name:"Dayang",middleName:null,surname:"Jawawi",slug:"dayang-jawawi",fullName:"Dayang Jawawi",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"University of Technology Malaysia",country:{name:"Malaysia"}}},{id:"528",title:"Dr.",name:"Kresimir",middleName:null,surname:"Delac",slug:"kresimir-delac",fullName:"Kresimir Delac",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/528/images/system/528.jpg",biography:"K. Delac received his B.Sc.E.E. degree in 2003 and is currentlypursuing a Ph.D. degree at the University of Zagreb, Faculty of Electrical Engineering andComputing. His current research interests are digital image analysis, pattern recognition andbiometrics.",institutionString:null,institution:{name:"University of Zagreb",country:{name:"Croatia"}}},{id:"557",title:"Dr.",name:"Andon",middleName:"Venelinov",surname:"Topalov",slug:"andon-topalov",fullName:"Andon Topalov",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/557/images/1927_n.jpg",biography:"Dr. Andon V. Topalov received the MSc degree in Control Engineering from the Faculty of Information Systems, Technologies, and Automation at Moscow State University of Civil Engineering (MGGU) in 1979. He then received his PhD degree in Control Engineering from the Department of Automation and Remote Control at Moscow State Mining University (MGSU), Moscow, in 1984. From 1985 to 1986, he was a Research Fellow in the Research Institute for Electronic Equipment, ZZU AD, Plovdiv, Bulgaria. In 1986, he joined the Department of Control Systems, Technical University of Sofia at the Plovdiv campus, where he is presently a Full Professor. He has held long-term visiting Professor/Scholar positions at various institutions in South Korea, Turkey, Mexico, Greece, Belgium, UK, and Germany. And he has coauthored one book and authored or coauthored more than 80 research papers in conference proceedings and journals. 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Most smart home systems are controlled by smartphones and microcontrollers. A smartphone application is used to control and monitor home functions using wireless communication techniques. We explore the concept of smart home with the integration of IoT services and cloud computing to it, by embedding intelligence into sensors and actuators, networking of smart things using the corresponding technology, facilitating interactions with smart things using cloud computing for easy access in different locations, increasing computation power, storage space and improving data exchange efficiency. In this chapter we present a composition of three components to build a robust approach of an advanced smart home concept and implementation.",book:{id:"7602",slug:"internet-of-things-iot-for-automated-and-smart-applications",title:"Internet of Things (IoT) for Automated and Smart Applications",fullTitle:"Internet of Things (IoT) for Automated and Smart Applications"},signatures:"Menachem Domb",authors:[{id:"222778",title:"Prof.",name:"Menachem",middleName:null,surname:"Domb",slug:"menachem-domb",fullName:"Menachem Domb"}]},{id:"62481",title:"Blockchain and Digital Currency in the World of Finance",slug:"blockchain-and-digital-currency-in-the-world-of-finance",totalDownloads:2052,totalCrossrefCites:4,totalDimensionsCites:5,abstract:"High-tech enables payment evolution and global competition. The ambiguities surrounding of the digital currency still leave enough space for the analysis of its unreserved acceptance, trust and anticipation, which are the main driver for the spread of the network. Banks should carefully consider the technology underlying these cryptocurrencies as a potential generic new way of transferring ownership of the value over the long term. The chapter provides an analysis of the use of cryptocurrencies in general, especially Bitcoin as the technology adoption in the presence of network externalities. The objective attitude is the future of the digital currency in the moment is still unsolved issue due to the existence of “critical mass”. Further, the chapter explores financial privacy which is very sensitive issue in using digital currency (or cryptocurrency) and discuss about private choices versus political rules. 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Islam",authors:[{id:"12623",title:"Prof.",name:"Mohammad Abdul",middleName:"A",surname:"Matin",slug:"mohammad-abdul-matin",fullName:"Mohammad Abdul Matin"}]},{id:"66938",title:"An Overview of Wireless Mesh Networks",slug:"an-overview-of-wireless-mesh-networks",totalDownloads:1693,totalCrossrefCites:2,totalDimensionsCites:5,abstract:"Wireless mesh networks (WMNs) are communication networks which comprise radio nodes in which nodes are arranged in a mesh topology. Mesh topology is an interconnection of all nodes connected with all other nodes in the network. The network includes devices like nodes, clients, routers, gateways, etc. As the nodes are fully connected, mesh networks are usually less mobile as rerouting is less difficult in predicting the reroute results in delay in data transmission. Mesh clients can be of any wireless devices like cell phones, laptops, etc. The gateways which act as forwarding nodes may not be connected with the Internet. As different devices come under a single network, it is also referred as mesh cloud. WMN is self-healable. It works better with various different networks which include cellular networks and IEEE 802.11, 802.15, and 802.16 as well. WMN is flexible to work with more than one protocol. This chapter gives architecture, layer functionalities, and applications.",book:{id:"7322",slug:"wireless-mesh-networks-security-architectures-and-protocols",title:"Wireless Mesh Networks",fullTitle:"Wireless Mesh Networks - Security, Architectures and Protocols"},signatures:"J. Rejina Parvin",authors:null},{id:"63090",title:"Cryptocurrency Returns",slug:"cryptocurrency-returns",totalDownloads:1471,totalCrossrefCites:0,totalDimensionsCites:0,abstract:"One of the most significant innovations in the world of finance has been the creation and evolvement of cryptocurrencies. These digital means of exchange have been the focus of extensive news coverage, especially the Bitcoin, with a primary focus on the tremendous potential return and the high level of accompanying risk. In this chapter, we examine the risk-return pattern for an array of cryptocurrencies, contrasting the pattern with those of conventional currency and equity investments. We find the measures of cryptocurrency returns and risk to be a very high multiple of those of conventional investments, and the pattern is determined to be robust relative to the time frame. Consequently, cryptocurrencies are determined to provide an alternative to investors that involves tremendously high risk and return.",book:{id:"7228",slug:"blockchain-and-cryptocurrencies",title:"Blockchain and Cryptocurrencies",fullTitle:"Blockchain and Cryptocurrencies"},signatures:"Mike Cudd, Kristen Ritterbush, Marcelo Eduardo and Chris Smith",authors:[{id:"254939",title:"Dr.",name:"Mike",middleName:null,surname:"Cudd",slug:"mike-cudd",fullName:"Mike Cudd"}]}],onlineFirstChaptersFilter:{topicId:"88",limit:6,offset:0},onlineFirstChaptersCollection:[],onlineFirstChaptersTotal:0},preDownload:{success:null,errors:{}},subscriptionForm:{success:null,errors:{}},aboutIntechopen:{},privacyPolicy:{},peerReviewing:{},howOpenAccessPublishingWithIntechopenWorks:{},sponsorshipBooks:{sponsorshipBooks:[],offset:8,limit:8,total:0},allSeries:{pteSeriesList:[{id:"14",title:"Artificial Intelligence",numberOfPublishedBooks:9,numberOfPublishedChapters:90,numberOfOpenTopics:6,numberOfUpcomingTopics:0,issn:"2633-1403",doi:"10.5772/intechopen.79920",isOpenForSubmission:!0},{id:"7",title:"Biomedical Engineering",numberOfPublishedBooks:12,numberOfPublishedChapters:107,numberOfOpenTopics:3,numberOfUpcomingTopics:0,issn:"2631-5343",doi:"10.5772/intechopen.71985",isOpenForSubmission:!0}],lsSeriesList:[{id:"11",title:"Biochemistry",numberOfPublishedBooks:33,numberOfPublishedChapters:330,numberOfOpenTopics:4,numberOfUpcomingTopics:0,issn:"2632-0983",doi:"10.5772/intechopen.72877",isOpenForSubmission:!0},{id:"25",title:"Environmental Sciences",numberOfPublishedBooks:1,numberOfPublishedChapters:19,numberOfOpenTopics:4,numberOfUpcomingTopics:0,issn:"2754-6713",doi:"10.5772/intechopen.100362",isOpenForSubmission:!0},{id:"10",title:"Physiology",numberOfPublishedBooks:14,numberOfPublishedChapters:145,numberOfOpenTopics:4,numberOfUpcomingTopics:0,issn:"2631-8261",doi:"10.5772/intechopen.72796",isOpenForSubmission:!0}],hsSeriesList:[{id:"3",title:"Dentistry",numberOfPublishedBooks:9,numberOfPublishedChapters:139,numberOfOpenTopics:2,numberOfUpcomingTopics:0,issn:"2631-6218",doi:"10.5772/intechopen.71199",isOpenForSubmission:!0},{id:"6",title:"Infectious Diseases",numberOfPublishedBooks:13,numberOfPublishedChapters:122,numberOfOpenTopics:4,numberOfUpcomingTopics:0,issn:"2631-6188",doi:"10.5772/intechopen.71852",isOpenForSubmission:!0},{id:"13",title:"Veterinary Medicine and Science",numberOfPublishedBooks:11,numberOfPublishedChapters:112,numberOfOpenTopics:3,numberOfUpcomingTopics:0,issn:"2632-0517",doi:"10.5772/intechopen.73681",isOpenForSubmission:!0}],sshSeriesList:[{id:"22",title:"Business, Management and Economics",numberOfPublishedBooks:1,numberOfPublishedChapters:21,numberOfOpenTopics:3,numberOfUpcomingTopics:0,issn:"2753-894X",doi:"10.5772/intechopen.100359",isOpenForSubmission:!0},{id:"23",title:"Education and Human Development",numberOfPublishedBooks:0,numberOfPublishedChapters:10,numberOfOpenTopics:1,numberOfUpcomingTopics:1,issn:null,doi:"10.5772/intechopen.100360",isOpenForSubmission:!0},{id:"24",title:"Sustainable Development",numberOfPublishedBooks:1,numberOfPublishedChapters:19,numberOfOpenTopics:5,numberOfUpcomingTopics:0,issn:"2753-6580",doi:"10.5772/intechopen.100361",isOpenForSubmission:!0}],testimonialsList:[{id:"13",text:"The collaboration with and support of the technical staff of IntechOpen is fantastic. 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Topics will include general overviews of infections, immunopathology, diagnosis, treatment, epidemiology, etiology, and current clinical recommendations for managing infectious diseases. Ongoing issues, recent advances, and future diagnostic approaches and therapeutic strategies will also be discussed. This book series will focus on various aspects and properties of infectious diseases whose deep understanding is essential for safeguarding the human race from losing resources and economies due to pathogens.",coverUrl:"https://cdn.intechopen.com/series/covers/6.jpg",latestPublicationDate:"August 2nd, 2022",hasOnlineFirst:!0,numberOfPublishedBooks:13,editor:{id:"131400",title:"Prof.",name:"Alfonso J.",middleName:null,surname:"Rodriguez-Morales",slug:"alfonso-j.-rodriguez-morales",fullName:"Alfonso J. 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He is an External Professor, Master in Research on Tropical Medicine and International Health, Universitat de Barcelona, Spain. He is also a professor at the Master in Clinical Epidemiology and Biostatistics, Universidad Científica del Sur, Lima, Peru. In 2021 he has been awarded the “Raul Isturiz Award” Medal of the API. Also, in 2021, he was awarded with the “Jose Felix Patiño” Asclepius Staff Medal of the Colombian Medical College, due to his scientific contributions to COVID-19 during the pandemic. He is currently the Editor in Chief of the journal Travel Medicine and Infectious Diseases. 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Other positions she has held at the university include Vice-Dean of Master Programs, Vice-Dean of the Degree in Biology and Vice-Dean for Mobility and Enterprise and Engagement at the Faculty of Science (University of Alicante). She received her Bachelor in Biology in 1998 (University of Alicante) and her PhD in 2003 (Biochemistry, University of Alicante). She undertook post-doctoral research at the University of East Anglia (Norwich, U.K. 2004-2005; 2007-2008).\nHer multidisciplinary research focuses on investigating archaea and their potential applications in biotechnology. She has an H-index of 21. She has authored one patent and has published more than 70 indexed papers and around 60 book chapters.\nShe has contributed to more than 150 national and international meetings during the last 15 years. Her research interests include archaea metabolism, enzymes purification and characterization, gene regulation, carotenoids and bioplastics production, antioxidant\ncompounds, waste water treatments, and brines bioremediation.\nRosa María’s other roles include editorial board member for several journals related\nto biochemistry, reviewer for more than 60 journals (biochemistry, molecular biology, biotechnology, chemistry and microbiology) and president of several organizing committees in international meetings related to the N-cycle or respiratory processes.",institutionString:null,institution:{name:"University of Alicante",institutionURL:null,country:{name:"Spain"}}},editorTwo:null,editorThree:null},{id:"15",title:"Chemical Biology",coverUrl:"https://cdn.intechopen.com/series_topics/covers/15.jpg",isOpenForSubmission:!0,editor:{id:"441442",title:"Dr.",name:"Şükrü",middleName:null,surname:"Beydemir",slug:"sukru-beydemir",fullName:"Şükrü Beydemir",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0033Y00003GsUoIQAV/Profile_Picture_1634557147521",biography:"Dr. Şükrü Beydemir obtained a BSc in Chemistry in 1995 from Yüzüncü Yıl University, MSc in Biochemistry in 1998, and PhD in Biochemistry in 2002 from Atatürk University, Turkey. He performed post-doctoral studies at Max-Planck Institute, Germany, and University of Florence, Italy in addition to making several scientific visits abroad. He currently works as a Full Professor of Biochemistry in the Faculty of Pharmacy, Anadolu University, Turkey. Dr. Beydemir has published over a hundred scientific papers spanning protein biochemistry, enzymology and medicinal chemistry, reviews, book chapters and presented several conferences to scientists worldwide. He has received numerous publication awards from various international scientific councils. He serves in the Editorial Board of several international journals. 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He is a member of the Turkish Biochemical Society, American Chemical Society, and German Genetics society. Dr. Ekinci published around ninety scientific papers, reviews and book chapters, and presented several conferences to scientists. He has received numerous publication awards from several scientific councils. 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He worked on the structure-function relationships of glycoconjugates and his main project was the investigations on the biological roles of the de-N-glycosylation enzymes (Endo-N-acetyl-β-D-glucosaminidase and peptide-N4-(N-acetyl-β-glucosaminyl) asparagine amidase). From 2002 he contributes to the understanding of the Blood-brain barrier functioning using proteomics approaches. He has published more than 70 papers. His teaching areas are energy metabolism and regulation, integration and organ specialization and metabolic adaptation.",institutionString:null,institution:{name:"Artois University",institutionURL:null,country:{name:"France"}}},editorTwo:null,editorThree:null},{id:"18",title:"Proteomics",coverUrl:"https://cdn.intechopen.com/series_topics/covers/18.jpg",isOpenForSubmission:!0,editor:{id:"200689",title:"Prof.",name:"Paolo",middleName:null,surname:"Iadarola",slug:"paolo-iadarola",fullName:"Paolo Iadarola",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bSCl8QAG/Profile_Picture_1623568118342",biography:"Paolo Iadarola graduated with a degree in Chemistry from the University of Pavia (Italy) in July 1972. He then worked as an Assistant Professor at the Faculty of Science of the same University until 1984. In 1985, Prof. Iadarola became Associate Professor at the Department of Biology and Biotechnologies of the University of Pavia and retired in October 2017. Since then, he has been working as an Adjunct Professor in the same Department at the University of Pavia. His research activity during the first years was primarily focused on the purification and structural characterization of enzymes from animal and plant sources. During this period, Prof. Iadarola familiarized himself with the conventional techniques used in column chromatography, spectrophotometry, manual Edman degradation, and electrophoresis). Since 1995, he has been working on: i) the determination in biological fluids (serum, urine, bronchoalveolar lavage, sputum) of proteolytic activities involved in the degradation processes of connective tissue matrix, and ii) on the identification of biological markers of lung diseases. In this context, he has developed and validated new methodologies (e.g., Capillary Electrophoresis coupled to Laser-Induced Fluorescence, CE-LIF) whose application enabled him to determine both the amounts of biochemical markers (Desmosines) in urine/serum of patients affected by Chronic Obstructive Pulmonary Disease (COPD) and the activity of proteolytic enzymes (Human Neutrophil Elastase, Cathepsin G, Pseudomonas aeruginosa elastase) in sputa of these patients. More recently, Prof. Iadarola was involved in developing techniques such as two-dimensional electrophoresis coupled to liquid chromatography/mass spectrometry (2DE-LC/MS) for the proteomic analysis of biological fluids aimed at the identification of potential biomarkers of different lung diseases. He is the author of about 150 publications (According to Scopus: H-Index: 23; Total citations: 1568- According to WOS: H-Index: 20; Total Citations: 1296) of peer-reviewed international journals. He is a Consultant Reviewer for several journals, including the Journal of Chromatography A, Journal of Chromatography B, Plos ONE, Proteomes, International Journal of Molecular Science, Biotech, Electrophoresis, and others. He is also Associate Editor of Biotech.",institutionString:null,institution:{name:"University of Pavia",institutionURL:null,country:{name:"Italy"}}},editorTwo:{id:"201414",title:"Dr.",name:"Simona",middleName:null,surname:"Viglio",slug:"simona-viglio",fullName:"Simona Viglio",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRKDHQA4/Profile_Picture_1630402531487",biography:"Simona Viglio is an Associate Professor of Biochemistry at the Department of Molecular Medicine at the University of Pavia. She has been working since 1995 on the determination of proteolytic enzymes involved in the degradation process of connective tissue matrix and on the identification of biological markers of lung diseases. She gained considerable experience in developing and validating new methodologies whose applications allowed her to determine both the amount of biomarkers (Desmosine and Isodesmosine) in the urine of patients affected by COPD, and the activity of proteolytic enzymes (HNE, Cathepsin G, Pseudomonas aeruginosa elastase) in the sputa of these patients. Simona Viglio was also involved in research dealing with the supplementation of amino acids in patients with brain injury and chronic heart failure. She is presently engaged in the development of 2-DE and LC-MS techniques for the study of proteomics in biological fluids. The aim of this research is the identification of potential biomarkers of lung diseases. She is an author of about 90 publications (According to Scopus: H-Index: 23; According to WOS: H-Index: 20) on peer-reviewed journals, a member of the “Società Italiana di Biochimica e Biologia Molecolare,“ and a Consultant Reviewer for International Journal of Molecular Science, Journal of Chromatography A, COPD, Plos ONE and Nutritional Neuroscience.",institutionString:null,institution:{name:"University of Pavia",institutionURL:null,country:{name:"Italy"}}},editorThree:null}]},overviewPageOFChapters:{paginationCount:42,paginationItems:[{id:"82914",title:"Glance on the Critical Role of IL-23 Receptor Gene Variations in Inflammation-Induced Carcinogenesis",doi:"10.5772/intechopen.105049",signatures:"Mohammed El-Gedamy",slug:"glance-on-the-critical-role-of-il-23-receptor-gene-variations-in-inflammation-induced-carcinogenesis",totalDownloads:8,totalCrossrefCites:0,totalDimensionsCites:0,authors:null,book:{title:"Chemokines Updates",coverURL:"https://cdn.intechopen.com/books/images_new/11672.jpg",subseries:{id:"18",title:"Proteomics"}}},{id:"82875",title:"Lipidomics as a Tool in the Diagnosis and Clinical Therapy",doi:"10.5772/intechopen.105857",signatures:"María Elizbeth Alvarez Sánchez, Erick Nolasco Ontiveros, Rodrigo Arreola, Adriana Montserrat Espinosa González, Ana María García Bores, Roberto Eduardo López Urrutia, Ignacio Peñalosa Castro, María del Socorro Sánchez Correa and Edgar Antonio Estrella Parra",slug:"lipidomics-as-a-tool-in-the-diagnosis-and-clinical-therapy",totalDownloads:7,totalCrossrefCites:0,totalDimensionsCites:0,authors:null,book:{title:"Fatty Acids - Recent Advances",coverURL:"https://cdn.intechopen.com/books/images_new/11669.jpg",subseries:{id:"17",title:"Metabolism"}}},{id:"82440",title:"Lipid Metabolism and Associated Molecular Signaling Events in Autoimmune Disease",doi:"10.5772/intechopen.105746",signatures:"Mohan Vanditha, Sonu Das and Mathew John",slug:"lipid-metabolism-and-associated-molecular-signaling-events-in-autoimmune-disease",totalDownloads:17,totalCrossrefCites:0,totalDimensionsCites:0,authors:null,book:{title:"Fatty Acids - Recent Advances",coverURL:"https://cdn.intechopen.com/books/images_new/11669.jpg",subseries:{id:"17",title:"Metabolism"}}},{id:"82483",title:"Oxidative Stress in Cardiovascular Diseases",doi:"10.5772/intechopen.105891",signatures:"Laura Mourino-Alvarez, Tamara Sastre-Oliva, Nerea Corbacho-Alonso and Maria G. 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He is an academic staff member of the Department of Reproduction and Artificial Insemination, Selçuk University, Turkey. He manages several studies on sperms and embryos and is an editorial board member for several international journals. His studies include sperm cryobiology, in vitro fertilization, and embryo production in animals.",institutionString:"Selçuk University, Faculty of Veterinary Medicine",institution:null},{id:"90846",title:"Prof.",name:"Yusuf",middleName:null,surname:"Bozkurt",slug:"yusuf-bozkurt",fullName:"Yusuf Bozkurt",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/90846/images/system/90846.jpg",biography:"Yusuf Bozkurt has a BSc, MSc, and Ph.D. from Ankara University, Turkey. He is currently a Professor of Biotechnology of Reproduction in the field of Aquaculture, İskenderun Technical University, Turkey. His research interests include reproductive biology and biotechnology with an emphasis on cryo-conservation. He is on the editorial board of several international peer-reviewed journals and has published many papers. Additionally, he has participated in many international and national congresses, seminars, and workshops with oral and poster presentations. He is an active member of many local and international organizations.",institutionString:"İskenderun Technical University",institution:{name:"İskenderun Technical University",country:{name:"Turkey"}}},{id:"61139",title:"Dr.",name:"Sergey",middleName:null,surname:"Tkachev",slug:"sergey-tkachev",fullName:"Sergey Tkachev",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/61139/images/system/61139.png",biography:"Dr. Sergey Tkachev is a senior research scientist at the Institute of Fundamental Medicine and Biology, Kazan Federal University, Russia, and at the Institute of Chemical Biology and Fundamental Medicine SB RAS, Novosibirsk, Russia. He received his Ph.D. in Molecular Biology with his thesis “Genetic variability of the tick-borne encephalitis virus in natural foci of Novosibirsk city and its suburbs.” His primary field is molecular virology with research emphasis on vector-borne viruses, especially tick-borne encephalitis virus, Kemerovo virus and Omsk hemorrhagic fever virus, rabies virus, molecular genetics, biology, and epidemiology of virus pathogens.",institutionString:"Russian Academy of Sciences",institution:{name:"Russian Academy of Sciences",country:{name:"Russia"}}},{id:"310962",title:"Dr.",name:"Amlan",middleName:"Kumar",surname:"Patra",slug:"amlan-patra",fullName:"Amlan Patra",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/310962/images/system/310962.jpg",biography:"Amlan K. Patra, FRSB, obtained a Ph.D. in Animal Nutrition from Indian Veterinary Research Institute, India, in 2002. He is currently an associate professor at West Bengal University of Animal and Fishery Sciences. He has more than twenty years of research and teaching experience. He held previous positions at the American Institute for Goat Research, The Ohio State University, Columbus, USA, and Free University of Berlin, Germany. His research focuses on animal nutrition, particularly ruminants and poultry nutrition, gastrointestinal electrophysiology, meta-analysis and modeling in nutrition, and livestock–environment interaction. He has authored around 175 articles in journals, book chapters, and proceedings. Dr. Patra serves on the editorial boards of several reputed journals.",institutionString:null,institution:{name:"West Bengal University of Animal and Fishery Sciences",country:{name:"India"}}},{id:"53998",title:"Prof.",name:"László",middleName:null,surname:"Babinszky",slug:"laszlo-babinszky",fullName:"László Babinszky",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/53998/images/system/53998.png",biography:"László Babinszky is Professor Emeritus, Department of Animal Nutrition Physiology, University of Debrecen, Hungary. He has also worked in the Department of Animal Nutrition, University of Wageningen, Netherlands; the Institute for Livestock Feeding and Nutrition (IVVO), Lelystad, Netherlands; the Agricultural University of Vienna (BOKU); the Institute for Animal Breeding and Nutrition, Austria; and the Oscar Kellner Research Institute for Animal Nutrition, Rostock, Germany. In 1992, Dr. Babinszky obtained a Ph.D. in Animal Nutrition from the University of Wageningen. His main research areas are swine and poultry nutrition. He has authored more than 300 publications (papers, book chapters) and edited four books and fourteen international conference proceedings.",institutionString:"University of Debrecen",institution:{name:"University of Debrecen",country:{name:"Hungary"}}},{id:"201830",title:"Dr.",name:"Fernando",middleName:"Sanchez",surname:"Davila",slug:"fernando-davila",fullName:"Fernando Davila",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/201830/images/5017_n.jpg",biography:"I am a professor at UANL since 1988. My research lines are the development of reproductive techniques in small ruminants. We also conducted research on sexual and social behavior in males.\nI am Mexican and study my professional career as an engineer in agriculture and animal science at UANL. Then take a masters degree in science in Germany (Animal breeding). Take a doctorate in animal science at the UANL.",institutionString:null,institution:{name:"Universidad Autónoma de Nuevo León",country:{name:"Mexico"}}},{id:"309250",title:"Dr.",name:"Miguel",middleName:null,surname:"Quaresma",slug:"miguel-quaresma",fullName:"Miguel Quaresma",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/309250/images/9059_n.jpg",biography:"Miguel Nuno Pinheiro Quaresma was born on May 26, 1974 in Dili, Timor Island. He is married with two children: a boy and a girl, and he is a resident in Vila Real, Portugal. He graduated in Veterinary Medicine in August 1998 and obtained his Ph.D. degree in Veterinary Sciences -Clinical Area in February 2015, both from the University of Trás-os-Montes e Alto Douro. He is currently enrolled in the Alternative Residency of the European College of Animal Reproduction. He works as a Senior Clinician at the Veterinary Teaching Hospital of UTAD (HVUTAD) with a role in clinical activity in the area of livestock and equine species as well as to support teaching and research in related areas. He teaches as an Invited Professor in Reproduction Medicine I and II of the Master\\'s in Veterinary Medicine degree at UTAD. Currently, he holds the position of Chairman of the Portuguese Buiatrics Association. He is a member of the Consultive Group on Production Animals of the OMV. He has 19 publications in indexed international journals (ISIS), as well as over 60 publications and oral presentations in both Portuguese and international journals and congresses.",institutionString:"University of Trás-os-Montes and Alto Douro",institution:{name:"University of Trás-os-Montes and Alto Douro",country:{name:"Portugal"}}},{id:"38652",title:"Prof.",name:"Rita",middleName:null,surname:"Payan-Carreira",slug:"rita-payan-carreira",fullName:"Rita Payan-Carreira",position:null,profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRiFPQA0/Profile_Picture_1614601496313",biography:"Rita Payan Carreira earned her Veterinary Degree from the Faculty of Veterinary Medicine in Lisbon, Portugal, in 1985. She obtained her Ph.D. in Veterinary Sciences from the University of Trás-os-Montes e Alto Douro, Portugal. After almost 32 years of teaching at the University of Trás-os-Montes and Alto Douro, she recently moved to the University of Évora, Department of Veterinary Medicine, where she teaches in the field of Animal Reproduction and Clinics. Her primary research areas include the molecular markers of the endometrial cycle and the embryo–maternal interaction, including oxidative stress and the reproductive physiology and disorders of sexual development, besides the molecular determinants of male and female fertility. She often supervises students preparing their master's or doctoral theses. She is also a frequent referee for various journals.",institutionString:null,institution:{name:"University of Évora",country:{name:"Portugal"}}},{id:"283019",title:"Dr.",name:"Oudessa",middleName:null,surname:"Kerro Dego",slug:"oudessa-kerro-dego",fullName:"Oudessa Kerro Dego",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/283019/images/system/283019.png",biography:"Dr. Kerro Dego is a veterinary microbiologist with training in veterinary medicine, microbiology, and anatomic pathology. Dr. Kerro Dego is an assistant professor of dairy health in the department of animal science, the University of Tennessee, Institute of Agriculture, Knoxville, Tennessee. He received his D.V.M. (1997), M.S. (2002), and Ph.D. (2008) degrees in Veterinary Medicine, Animal Pathology and Veterinary Microbiology from College of Veterinary Medicine, Addis Ababa University, Ethiopia; College of Veterinary Medicine, Utrecht University, the Netherlands and Western College of Veterinary Medicine, University of Saskatchewan, Canada respectively. He did his Postdoctoral training in microbial pathogenesis (2009 - 2015) in the Department of Animal Science, the University of Tennessee, Institute of Agriculture, Knoxville, Tennessee. Dr. Kerro Dego’s research focuses on the prevention and control of infectious diseases of farm animals, particularly mastitis, improving dairy food safety, and mitigation of antimicrobial resistance. Dr. Kerro Dego has extensive experience in studying the pathogenesis of bacterial infections, identification of virulence factors, and vaccine development and efficacy testing against major bacterial mastitis pathogens. Dr. Kerro Dego conducted numerous controlled experimental and field vaccine efficacy studies, vaccination, and evaluation of immunological responses in several species of animals, including rodents (mice) and large animals (bovine and ovine).",institutionString:"University of Tennessee at Knoxville",institution:{name:"University of Tennessee at Knoxville",country:{name:"United States of America"}}},{id:"251314",title:"Dr.",name:"Juan Carlos",middleName:null,surname:"Gardón Poggi",slug:"juan-carlos-gardon-poggi",fullName:"Juan Carlos Gardón Poggi",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/251314/images/system/251314.jpeg",biography:"Juan Carlos Gardón Poggi received University degree from the Faculty of Agrarian Science in Argentina, in 1983. Also he received Masters Degree and PhD from Córdoba University, Spain. He is currently a Professor at the Catholic University of Valencia San Vicente Mártir, at the Department of Medicine and Animal Surgery. He teaches diverse courses in the field of Animal Reproduction and he is the Director of the Veterinary Farm. He also participates in academic postgraduate activities at the Veterinary Faculty of Murcia University, Spain. His research areas include animal physiology, physiology and biotechnology of reproduction either in males or females, the study of gametes under in vitro conditions and the use of ultrasound as a complement to physiological studies and development of applied biotechnologies. Routinely, he supervises students preparing their doctoral, master thesis or final degree projects.",institutionString:null,institution:{name:"Valencia Catholic University Saint Vincent Martyr",country:{name:"Spain"}}},{id:"309529",title:"Dr.",name:"Albert",middleName:null,surname:"Rizvanov",slug:"albert-rizvanov",fullName:"Albert Rizvanov",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/309529/images/9189_n.jpg",biography:'Albert A. Rizvanov is a Professor and Director of the Center for Precision and Regenerative Medicine at the Institute of Fundamental Medicine and Biology, Kazan Federal University (KFU), Russia. He is the Head of the Center of Excellence “Regenerative Medicine” and Vice-Director of Strategic Academic Unit \\"Translational 7P Medicine\\". Albert completed his Ph.D. at the University of Nevada, Reno, USA and Dr.Sci. at KFU. He is a corresponding member of the Tatarstan Academy of Sciences, Russian Federation. Albert is an author of more than 300 peer-reviewed journal articles and 22 patents. He has supervised 11 Ph.D. and 2 Dr.Sci. dissertations. Albert is the Head of the Dissertation Committee on Biochemistry, Microbiology, and Genetics at KFU.\nORCID https://orcid.org/0000-0002-9427-5739\nWebsite https://kpfu.ru/Albert.Rizvanov?p_lang=2',institutionString:"Kazan Federal University",institution:{name:"Kazan Federal University",country:{name:"Russia"}}},{id:"210551",title:"Dr.",name:"Arbab",middleName:null,surname:"Sikandar",slug:"arbab-sikandar",fullName:"Arbab Sikandar",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/210551/images/system/210551.jpg",biography:"Dr. Arbab Sikandar, PhD, M. Phil, DVM was born on April 05, 1981. He is currently working at the College of Veterinary & Animal Sciences as an Assistant Professor. He previously worked as a lecturer at the same University. \nHe is a Member/Secretory of Ethics committee (No. CVAS-9377 dated 18-04-18), Member of the QEC committee CVAS, Jhang (Regr/Gen/69/873, dated 26-10-2017), Member, Board of studies of Department of Basic Sciences (No. CVAS. 2851 Dated. 12-04-13, and No. CVAS, 9024 dated 20/11/17), Member of Academic Committee, CVAS, Jhang (No. CVAS/2004, Dated, 25-08-12), Member of the technical committee (No. CVAS/ 4085, dated 20,03, 2010 till 2016).\n\nDr. Arbab Sikandar contributed in five days hands-on-training on Histopathology at the Department of Pathology, UVAS from 12-16 June 2017. He received a Certificate of appreciation for contributions for Popularization of Science and Technology in the Society on 17-11-15. He was the resource person in the lecture series- ‘scientific writing’ at the Department of Anatomy and Histology, UVAS, Lahore on 29th October 2015. He won a full fellowship as a principal candidate for the year 2015 in the field of Agriculture, EICA, Egypt with ref. to the Notification No. 12(11) ACS/Egypt/2014 from 10 July 2015 to 25th September 2015.; he received a grant of Rs. 55000/- as research incentives from Director, Advanced Studies and Research, UVAS, Lahore upon publications of research papers in IF Journals (DR/215, dated 19-5-2014.. He obtained his PhD by winning a HEC Pakistan indigenous Scholarship, ‘Ph.D. fellowship for 5000 scholars – Phase II’ (2av1-147), 17-6/HEC/HRD/IS-II/12, November 15, 2012. \n\nDr. Sikandar is a member of numerous societies: Registered Veterinary Medical Practitioner (life member) and Registered Veterinary Medical Faculty of Pakistan Veterinary Medical Council. The Registration code of PVMC is RVMP/4298 and RVMF/ 0102.; Life member of the University of Veterinary and Animal Sciences, Lahore, Alumni Association with S# 664, dated: 6-4-12. ; Member 'Vets Care Organization Pakistan” with Reference No. VCO-605-149, dated 05-04-06. :Member 'Vet Crescent” (Society of Animal Health and Production), UVAS, Lahore.",institutionString:"University of Veterinary & Animal Science",institution:{name:"University of Veterinary and Animal Sciences",country:{name:"Pakistan"}}},{id:"311663",title:"Dr.",name:"Prasanna",middleName:null,surname:"Pal",slug:"prasanna-pal",fullName:"Prasanna Pal",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/311663/images/13261_n.jpg",biography:null,institutionString:null,institution:{name:"National Dairy Research Institute",country:{name:"India"}}},{id:"202192",title:"Dr.",name:"Catrin",middleName:null,surname:"Rutland",slug:"catrin-rutland",fullName:"Catrin Rutland",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/202192/images/system/202192.png",biography:"Catrin Rutland is an Associate Professor of Anatomy and Developmental Genetics at the University of Nottingham, UK. She obtained a BSc from the University of Derby, England, a master’s degree from Technische Universität München, Germany, and a Ph.D. from the University of Nottingham. She undertook a post-doctoral research fellowship in the School of Medicine before accepting tenure in Veterinary Medicine and Science. Dr. Rutland also obtained an MMedSci (Medical Education) and a Postgraduate Certificate in Higher Education (PGCHE). She is the author of more than sixty peer-reviewed journal articles, twelve books/book chapters, and more than 100 research abstracts in cardiovascular biology and oncology. She is a board member of the European Association of Veterinary Anatomists, Fellow of the Anatomical Society, and Senior Fellow of the Higher Education Academy. Dr. Rutland has also written popular science books for the public. https://orcid.org/0000-0002-2009-4898. www.nottingham.ac.uk/vet/people/catrin.rutland",institutionString:null,institution:{name:"University of Nottingham",country:{name:"United Kingdom"}}},{id:"283315",title:"Prof.",name:"Samir",middleName:null,surname:"El-Gendy",slug:"samir-el-gendy",fullName:"Samir El-Gendy",position:null,profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRduYQAS/Profile_Picture_1606215849748",biography:"Samir El-Gendy is a Professor of anatomy and embryology at the faculty of veterinary medicine, Alexandria University, Egypt. Samir obtained his PhD in veterinary science in 2007 from the faculty of veterinary medicine, Alexandria University and has been a professor since 2017. Samir is an author on 24 articles at Scopus and 12 articles within local journals and 2 books/book chapters. His research focuses on applied anatomy, imaging techniques and computed tomography. Samir worked as a member of different local projects on E-learning and he is a board member of the African Association of Veterinary Anatomists and of anatomy societies and as an associated author at local and international journals. Orcid: https://orcid.org/0000-0002-6180-389X",institutionString:null,institution:{name:"Alexandria University",country:{name:"Egypt"}}},{id:"246149",title:"Dr.",name:"Valentina",middleName:null,surname:"Kubale",slug:"valentina-kubale",fullName:"Valentina Kubale",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/246149/images/system/246149.jpg",biography:"Valentina Kubale is Associate Professor of Veterinary Medicine at the Veterinary Faculty, University of Ljubljana, Slovenia. Since graduating from the Veterinary faculty she obtained her PhD in 2007, performed collaboration with the Department of Pharmacology, University of Copenhagen, Denmark. She continued as a post-doctoral fellow at the University of Copenhagen with a Lundbeck foundation fellowship. She is the editor of three books and author/coauthor of 23 articles in peer-reviewed scientific journals, 16 book chapters, and 68 communications at scientific congresses. Since 2008 she has been the Editor Assistant for the Slovenian Veterinary Research journal. She is a member of Slovenian Biochemical Society, The Endocrine Society, European Association of Veterinary Anatomists and Society for Laboratory Animals, where she is board member.",institutionString:"University of Ljubljana",institution:{name:"University of Ljubljana",country:{name:"Slovenia"}}},{id:"258334",title:"Dr.",name:"Carlos Eduardo",middleName:null,surname:"Fonseca-Alves",slug:"carlos-eduardo-fonseca-alves",fullName:"Carlos Eduardo Fonseca-Alves",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/258334/images/system/258334.jpg",biography:"Dr. Fonseca-Alves earned his DVM from Federal University of Goias – UFG in 2008. He completed an internship in small animal internal medicine at UPIS university in 2011, earned his MSc in 2013 and PhD in 2015 both in Veterinary Medicine at Sao Paulo State University – UNESP. Dr. Fonseca-Alves currently serves as an Assistant Professor at Paulista University – UNIP teaching small animal internal medicine.",institutionString:null,institution:{name:"Universidade Paulista",country:{name:"Brazil"}}},{id:"245306",title:"Dr.",name:"María Luz",middleName:null,surname:"Garcia Pardo",slug:"maria-luz-garcia-pardo",fullName:"María Luz Garcia Pardo",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/245306/images/system/245306.png",biography:"María de la Luz García Pardo is an agricultural engineer from Universitat Politècnica de València, Spain. She has a Ph.D. in Animal Genetics. Currently, she is a lecturer at the Agrofood Technology Department of Miguel Hernández University, Spain. Her research is focused on genetics and reproduction in rabbits. The major goal of her research is the genetics of litter size through novel methods such as selection by the environmental sensibility of litter size, with forays into the field of animal welfare by analysing the impact on the susceptibility to diseases and stress of the does. Details of her publications can be found at https://orcid.org/0000-0001-9504-8290.",institutionString:null,institution:{name:"Miguel Hernandez University",country:{name:"Spain"}}},{id:"350704",title:"M.Sc.",name:"Camila",middleName:"Silva Costa",surname:"Ferreira",slug:"camila-ferreira",fullName:"Camila Ferreira",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/350704/images/17280_n.jpg",biography:"Graduated in Veterinary Medicine at the Fluminense Federal University, specialist in Equine Reproduction at the Brazilian Veterinary Institute (IBVET) and Master in Clinical Veterinary Medicine and Animal Reproduction at the Fluminense Federal University. She has experience in analyzing zootechnical indices in dairy cattle and organizing events related to Veterinary Medicine through extension grants. I have experience in the field of diagnostic imaging and animal reproduction in veterinary medicine through monitoring and scientific initiation scholarships. I worked at the Equus Central Reproduction Equine located in Santo Antônio de Jesus – BA in the 2016/2017 breeding season. I am currently a doctoral student with a scholarship from CAPES of the Postgraduate Program in Veterinary Medicine (Pathology and Clinical Sciences) at the Federal Rural University of Rio de Janeiro (UFRRJ) with a research project with an emphasis on equine endometritis.",institutionString:null,institution:null},{id:"41319",title:"Prof.",name:"Lung-Kwang",middleName:null,surname:"Pan",slug:"lung-kwang-pan",fullName:"Lung-Kwang Pan",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/41319/images/84_n.jpg",biography:null,institutionString:null,institution:null},{id:"125292",title:"Dr.",name:"Katy",middleName:null,surname:"Satué Ambrojo",slug:"katy-satue-ambrojo",fullName:"Katy Satué Ambrojo",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/125292/images/system/125292.jpeg",biography:"Katy Satué Ambrojo received her Veterinary Medicine degree, Master degree in Equine Technology and doctorate in Veterinary Medicine from the Faculty of Veterinary, CEU-Cardenal Herrera University in Valencia, Spain.Dr. Satué is accredited as a Private University Doctor Professor, Doctor Assistant, and Contracted Doctor by AVAP (Agència Valenciana d'Avaluació i Prospectiva) and currently, as a full professor by ANECA (since January 2022). To date, Katy has taught 22 years in the Department of Animal Medicine and Surgery at the CEU-Cardenal Herrera University in undergraduate courses in Veterinary Medicine (General Pathology, integrated into the Applied Basis of Veterinary Medicine module of the 2nd year, Clinical Equine I of 3rd year, and Equine Clinic II of 4th year). Dr. Satué research activity is in the field of Endocrinology, Hematology, Biochemistry, and Immunology in the Spanish Purebred mare. She has directed 5 Doctoral Theses and 5 Diplomas of Advanced Studies, and participated in 11 research projects as a collaborating researcher. She has written 2 books and 14 book chapters in international publishers related to the area, and 68 scientific publications in international journals. Dr. Satué has attended 63 congresses, participating with 132 communications in international congresses and 19 in national congresses related to the area. Dr. Satué is a scientific reviewer for various prestigious international journals such as Animals, American Journal of Obstetrics and Gynecology, Veterinary Clinical Pathology, Journal of Equine Veterinary Science, Reproduction in Domestic Animals, Research Veterinary Science, Brazilian Journal of Medical and Biological Research, Livestock Production Science and Theriogenology, among others. Since 2014 she has been responsible for the Clinical Analysis Laboratory of the CEU-Cardenal Herrera University Veterinary Clinical Hospital.",institutionString:null,institution:null},{id:"201721",title:"Dr.",name:"Beatrice",middleName:null,surname:"Funiciello",slug:"beatrice-funiciello",fullName:"Beatrice Funiciello",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/201721/images/11089_n.jpg",biography:"Graduated from the University of Milan in 2011, my post-graduate education included CertAVP modules mainly on equines (dermatology and internal medicine) and a few on small animal (dermatology and anaesthesia) at the University of Liverpool. After a general CertAVP (2015) I gained the designated Certificate in Veterinary Dermatology (2017) after taking the synoptic examination and then applied for the RCVS ADvanced Practitioner status. After that, I completed the Postgraduate Diploma in Veterinary Professional Studies at the University of Liverpool (2018). My main area of work is cross-species veterinary dermatology.",institutionString:null,institution:null},{id:"291226",title:"Dr.",name:"Monica",middleName:null,surname:"Cassel",slug:"monica-cassel",fullName:"Monica Cassel",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/291226/images/8232_n.jpg",biography:'Degree in Biological Sciences at the Federal University of Mato Grosso with scholarship for Scientific Initiation by FAPEMAT (2008/1) and CNPq (2008/2-2009/2): Project \\"Histological evidence of reproductive activity in lizards of the Manso region, Chapada dos Guimarães, Mato Grosso, Brazil\\". Master\\\'s degree in Ecology and Biodiversity Conservation at Federal University of Mato Grosso with a scholarship by CAPES/REUNI program: Project \\"Reproductive biology of Melanorivulus punctatus\\". PhD\\\'s degree in Science (Cell and Tissue Biology Area) \n at University of Sao Paulo with scholarship granted by FAPESP; Project \\"Development of morphofunctional changes in ovary of Astyanax altiparanae Garutti & Britski, 2000 (Teleostei, Characidae)\\". She has experience in Reproduction of vertebrates and Morphology, with emphasis in Cellular Biology and Histology. She is currently a teacher in the medium / technical level courses at IFMT-Alta Floresta, as well as in the Bachelor\\\'s degree in Animal Science and in the Bachelor\\\'s degree in Business.',institutionString:null,institution:null},{id:"442807",title:"Dr.",name:"Busani",middleName:null,surname:"Moyo",slug:"busani-moyo",fullName:"Busani Moyo",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"Gwanda State University",country:{name:"Zimbabwe"}}},{id:"439435",title:"Dr.",name:"Feda S.",middleName:null,surname:"Aljaser",slug:"feda-s.-aljaser",fullName:"Feda S. 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\r\n\tThe era of antibiotics led us to the illusion that the problem of bacterial infection is over. However, bacterial flexibility and adaptation mechanisms allow them to survive and grow in extreme conditions. The best example is the formation of a sophisticated society of bacteria defined as a biofilm. Understanding the mechanism of bacterial biofilm formation has changed our perception of the development of bacterial infection but successfully eradicating biofilm remains a challenge. Considering the above, it is not surprising that bacteria remain a major public health threat despite the development of many groups of antibiotics. Additionally, increasing prevalence of acquired antibiotic resistance forces us to realize that we are far from controlling the development of bacterial infections. On the other hand, many infections are endogenous and result from an unbalanced relationship between the host and the microorganism. The increasing use of immunosuppressants, such as chemotherapy or organ transplantation, increases the incidence of patients highly susceptible to bacterial infections in the population.
\r\n
\r\n\tThis topic will focus on the current challenges and advantages in the diagnosis and treatment of bacterial infections. We will discuss the host-microbiota relationship, the treatment of chronic infections due to biofilm formation, and the development of new diagnostic tools to rapidly distinguish between colonization and probable infection.
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Since many years, he is a member of steering committee of Gdańsk branch of Polish Society of Microbiologists, a member of ESCMID. He is also a reviewer and a member of editorial boards of a number of international journals.",institutionString:"Medical University of Gdańsk, Poland",institution:null},editorTwo:{id:"484980",title:"Dr.",name:"Katarzyna",middleName:null,surname:"Garbacz",slug:"katarzyna-garbacz",fullName:"Katarzyna Garbacz",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0033Y00003St8TAQAZ/Profile_Picture_2022-07-07T09:45:16.jpg",biography:"Katarzyna Maria Garbacz, MD, is an Associate Professor at the Medical University of Gdańsk, Poland and she is head of the Department of Oral Microbiology of the Medical University of Gdańsk. She has published more than 50 scientific publications in peer-reviewed journals. She has been a project leader funded by the National Science Centre of Poland. Prof. Garbacz is a microbiologist working on applied and fundamental questions in microbial epidemiology and pathogenesis. Her research interest is in antibiotic resistance, host-pathogen interaction, and therapeutics development for staphylococcal pathogens, mainly Staphylococcus aureus, which causes hospital-acquired infections. Currently, her research is mostly focused on the study of oral pathogens, particularly Staphylococcus spp.",institutionString:"Medical University of Gdańsk, Poland",institution:null},editorThree:null,series:{id:"6",title:"Infectious Diseases",doi:"10.5772/intechopen.71852",issn:"2631-6188"},editorialBoard:[{id:"190041",title:"Dr.",name:"Jose",middleName:null,surname:"Gutierrez Fernandez",slug:"jose-gutierrez-fernandez",fullName:"Jose Gutierrez Fernandez",profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",institutionString:null,institution:{name:"University of Granada",institutionURL:null,country:{name:"Spain"}}},{id:"156556",title:"Prof.",name:"Maria Teresa",middleName:null,surname:"Mascellino",slug:"maria-teresa-mascellino",fullName:"Maria Teresa Mascellino",profilePictureURL:"https://mts.intechopen.com/storage/users/156556/images/system/156556.jpg",institutionString:"Sapienza University",institution:{name:"Sapienza University of Rome",institutionURL:null,country:{name:"Italy"}}},{id:"164933",title:"Prof.",name:"Mónica Alexandra",middleName:null,surname:"Sousa Oleastro",slug:"monica-alexandra-sousa-oleastro",fullName:"Mónica Alexandra Sousa Oleastro",profilePictureURL:"https://mts.intechopen.com/storage/users/164933/images/system/164933.jpeg",institutionString:"National Institute of Health Dr Ricardo Jorge",institution:{name:"National Institute of Health Dr. Ricardo Jorge",institutionURL:null,country:{name:"Portugal"}}}]},onlineFirstChapters:{paginationCount:5,paginationItems:[{id:"82701",title:"Pathology of Streptococcal Infections",doi:"10.5772/intechopen.105814",signatures:"Yutaka Tsutsumi",slug:"pathology-of-streptococcal-infections",totalDownloads:8,totalCrossrefCites:0,totalDimensionsCites:0,authors:[{name:"Yutaka",surname:"Tsutsumi"}],book:{title:"Streptococcal Infections",coverURL:"https://cdn.intechopen.com/books/images_new/10828.jpg",subseries:{id:"3",title:"Bacterial Infectious Diseases"}}},{id:"82634",title:"Bacterial Sexually Transmitted Disease",doi:"10.5772/intechopen.105747",signatures:"Lebeza Alemu Tenaw",slug:"bacterial-sexually-transmitted-disease",totalDownloads:12,totalCrossrefCites:0,totalDimensionsCites:0,authors:null,book:{title:"Bacterial Sexually Transmitted Infections - 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