WTP surveys about forest areas with mainly non-use values.
\\n\\n
Released this past November, the list is based on data collected from the Web of Science and highlights some of the world’s most influential scientific minds by naming the researchers whose publications over the previous decade have included a high number of Highly Cited Papers placing them among the top 1% most-cited.
\\n\\nWe wish to congratulate all of the researchers named and especially our authors on this amazing accomplishment! We are happy and proud to share in their success!
Note: Edited in March 2021
\\n"}]',published:!0,mainMedia:{caption:"Highly Cited",originalUrl:"/media/original/117"}},components:[{type:"htmlEditorComponent",content:'IntechOpen is proud to announce that 191 of our authors have made the Clarivate™ Highly Cited Researchers List for 2020, ranking them among the top 1% most-cited.
\n\nThroughout the years, the list has named a total of 261 IntechOpen authors as Highly Cited. Of those researchers, 69 have been featured on the list multiple times.
\n\n\n\nReleased this past November, the list is based on data collected from the Web of Science and highlights some of the world’s most influential scientific minds by naming the researchers whose publications over the previous decade have included a high number of Highly Cited Papers placing them among the top 1% most-cited.
\n\nWe wish to congratulate all of the researchers named and especially our authors on this amazing accomplishment! We are happy and proud to share in their success!
Note: Edited in March 2021
\n'}],latestNews:[{slug:"webinar-introduction-to-open-science-wednesday-18-may-1-pm-cest-20220518",title:"Webinar: Introduction to Open Science | Wednesday 18 May, 1 PM CEST"},{slug:"step-in-the-right-direction-intechopen-launches-a-portfolio-of-open-science-journals-20220414",title:"Step in the Right Direction: IntechOpen Launches a Portfolio of Open Science Journals"},{slug:"let-s-meet-at-london-book-fair-5-7-april-2022-olympia-london-20220321",title:"Let’s meet at London Book Fair, 5-7 April 2022, Olympia London"},{slug:"50-books-published-as-part-of-intechopen-and-knowledge-unlatched-ku-collaboration-20220316",title:"50 Books published as part of IntechOpen and Knowledge Unlatched (KU) Collaboration"},{slug:"intechopen-joins-the-united-nations-sustainable-development-goals-publishers-compact-20221702",title:"IntechOpen joins the United Nations Sustainable Development Goals Publishers Compact"},{slug:"intechopen-signs-exclusive-representation-agreement-with-lsr-libros-servicios-y-representaciones-s-a-de-c-v-20211123",title:"IntechOpen Signs Exclusive Representation Agreement with LSR Libros Servicios y Representaciones S.A. de C.V"},{slug:"intechopen-expands-partnership-with-research4life-20211110",title:"IntechOpen Expands Partnership with Research4Life"},{slug:"introducing-intechopen-book-series-a-new-publishing-format-for-oa-books-20210915",title:"Introducing IntechOpen Book Series - A New Publishing Format for OA Books"}]},book:{item:{type:"book",id:"5991",leadTitle:null,fullTitle:"Natural Killer Cells",title:"Natural Killer Cells",subtitle:null,reviewType:"peer-reviewed",abstract:"The book Natural Killer Cells is the result of a collective work that addresses in a clear and comprehensive way for readers and through as many sensuous details as possible, the most and various fundamental aspects of natural killer cells, as well as their clinical applications in cancer immunotherapy. This book will serve as an invaluable resource and pedagogical support for clinicians, researchers, basic scientists, immunology and immunopathology lecturers, as well as for students in biology and medicine, especially the ones with an advanced understanding of immunology.",isbn:"978-953-51-3672-9",printIsbn:"978-953-51-3671-2",pdfIsbn:"978-953-51-4573-8",doi:"10.5772/66568",price:119,priceEur:129,priceUsd:155,slug:"natural-killer-cells",numberOfPages:208,isOpenForSubmission:!1,isInWos:null,isInBkci:!1,hash:"ea5a1d2f5030a6af3f29cc75fdb9f559",bookSignature:"Mourad Aribi",publishedDate:"December 13th 2017",coverURL:"https://cdn.intechopen.com/books/images_new/5991.jpg",numberOfDownloads:15492,numberOfWosCitations:13,numberOfCrossrefCitations:11,numberOfCrossrefCitationsByBook:1,numberOfDimensionsCitations:17,numberOfDimensionsCitationsByBook:1,hasAltmetrics:1,numberOfTotalCitations:41,isAvailableForWebshopOrdering:!0,dateEndFirstStepPublish:"November 17th 2016",dateEndSecondStepPublish:"December 8th 2016",dateEndThirdStepPublish:"September 17th 2017",dateEndFourthStepPublish:"October 17th 2017",dateEndFifthStepPublish:"December 17th 2017",currentStepOfPublishingProcess:5,indexedIn:"1,2,3,4,5,6",editedByType:"Edited by",kuFlag:!1,featuredMarkup:null,editors:[{id:"40046",title:"Prof.",name:"Mourad",middleName:null,surname:"Aribi",slug:"mourad-aribi",fullName:"Mourad Aribi",profilePictureURL:"https://mts.intechopen.com/storage/users/40046/images/system/40046.jpeg",biography:"Dr. Mourad Aribi, PhD, Dr. Hab., HDR, is a professor of immunology at the University of Tlemcen (Algeria), and the founder\r\nand director of the Laboratory of Applied Molecular Biology\r\nand Immunology (W0414100). His creativity allowed him to\r\nconstruct for the first time Master’s and PhD training programs\r\nin immunology at his university, welcoming students and young\r\nresearchers from different regions and countries. His current\r\nresearch focuses on the modulation of cell-mediated and inflammatory immune\r\nresponses in autoimmune diseases, cancer diseases, and infectious diseases. Thanks\r\nto his interdisciplinary skills, he was able to develop numerous high-level bilateral\r\nand multilateral collaboration projects with large teams, in particular with partners from CNRS and INSERM (Montpellier, Marseille, Burgundy-Franche-Comté,\r\nFrance), Institute for Immunodeficiency (Freibourg, Germany), and, more recently, with partners from Harvard Medical School (Boston, USA). He is a regular\r\nreviewer for many international scientific journals and is also a member of the\r\neditorial board of Frontiers in Immunology (the official journal of the International\r\nUnion of Immunological Societies).",institutionString:"University of Tlemcen",position:null,outsideEditionCount:0,totalCites:0,totalAuthoredChapters:"5",totalChapterViews:"0",totalEditedBooks:"3",institution:{name:"University of Abou Bekr Belkaïd",institutionURL:null,country:{name:"Algeria"}}}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null,coeditorOne:null,coeditorTwo:null,coeditorThree:null,coeditorFour:null,coeditorFive:null,topics:[{id:"899",title:"Cancer Immunology",slug:"pure-immunology-cancer-immunology"}],chapters:[{id:"57777",title:"Introductory Chapter: A Brief Overview on Natural Killer Cells",doi:"10.5772/intechopen.72328",slug:"introductory-chapter-a-brief-overview-on-natural-killer-cells",totalDownloads:1638,totalCrossrefCites:2,totalDimensionsCites:4,hasAltmetrics:0,abstract:null,signatures:"Mourad Aribi",downloadPdfUrl:"/chapter/pdf-download/57777",previewPdfUrl:"/chapter/pdf-preview/57777",authors:[{id:"40046",title:"Prof.",name:"Mourad",surname:"Aribi",slug:"mourad-aribi",fullName:"Mourad Aribi"}],corrections:null},{id:"55937",title:"NK Cells and Cancer",doi:"10.5772/intechopen.69658",slug:"nk-cells-and-cancer",totalDownloads:1684,totalCrossrefCites:1,totalDimensionsCites:1,hasAltmetrics:1,abstract:"NK cells play an important role in host immunity against cancer by exerting cytotoxicity and secreting a wide variety of cytokines to inhibit tumour progression. Their effector functions are regulated by the integration of opposing signals from activating and inhibitory receptors, which determine NK cell activity against tumour targets. NK cell cytotoxicity requires successful progression through discrete activation events that begin with NK cell adhesion to a tumour target cell and culminate in the polarized release of cytotoxic granules into the immunological synapse. Tumour cells can evade NK cell attack through numerous mechanisms such as shedding of activating ligands, upregulation of inhibitory ligands, or stimulation of inhibitory regulatory T lymphocytes. A better understanding of specific NK cell responses to tumour targets can generate better NK cell‐based immunotherapeutic strategies for cancer. This chapter discusses NK cell immunosurveillance of cancer, NK cell tumour recognition strategies, cancer immune evasion from NK cells, and different approaches to NK cell modulation for cancer therapy.",signatures:"May Sabry and Mark W. Lowdell",downloadPdfUrl:"/chapter/pdf-download/55937",previewPdfUrl:"/chapter/pdf-preview/55937",authors:[{id:"201842",title:"Dr.",name:"May",surname:"Sabry",slug:"may-sabry",fullName:"May Sabry"},{id:"207299",title:"Prof.",name:"Mark",surname:"Lowdell",slug:"mark-lowdell",fullName:"Mark Lowdell"}],corrections:null},{id:"57058",title:"Retracted: Natural Killer Cells in the Near Future of Immuno-Oncological Therapeutic Approaches",doi:"10.5772/intechopen.70567",slug:"natural-killer-cells-in-the-near-future-of-immuno-oncological-therapeutic-approaches",totalDownloads:1187,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:0,abstract:null,signatures:"Hend Mohamed El Tayebi",downloadPdfUrl:"/chapter/pdf-download/57058",previewPdfUrl:"/chapter/pdf-preview/57058",authors:[{id:"188076",title:"Dr.",name:"Hend M.",surname:"El Tayebi",slug:"hend-m.-el-tayebi",fullName:"Hend M. El Tayebi"}],corrections:null},{id:"57230",title:"NK Cells in Cancer Immunotherapy",doi:"10.5772/intechopen.71217",slug:"nk-cells-in-cancer-immunotherapy",totalDownloads:1845,totalCrossrefCites:0,totalDimensionsCites:1,hasAltmetrics:0,abstract:"Natural killer (NK) cells are crucial components of the innate immune system and play critical roles in host immunity against viral infections and cancer. NK cells’ activity is controlled by the interaction of a wide range of receptors expressed on their surfaces with cell surface ligands. Opposite signals delivered by inhibitory and activating receptors tightly regulate NK cells’ cytotoxicity. Natural killer cells can discriminate between normal and cancer cells. NK cells are known to directly recognize and kill malignant cells or induce apoptosis. However, tumor cells have the ability to evade those attacks. The main mechanisms involve the lack of expression or downregulation of the expression of major histocompatibility complex (MHC) class I molecules and secretion of soluble NKG2D ligands by tumor cells. Furthermore, tumors harbor a population of cancer stem cells (CSCs), which can drive tumor progression and therapeutical resistance. This chapter highlights the roles of NK cells in tumor immunosurveillance and their applications for cancer immunotherapy. NK cell biology and function as well as the role of their receptor interactions will be described. We will discuss the therapeutic applications of NK cells in cancer and NK cells targeting CSCs as a promising strategy for cancer therapy.",signatures:"Lynda Addou-Klouche",downloadPdfUrl:"/chapter/pdf-download/57230",previewPdfUrl:"/chapter/pdf-preview/57230",authors:[{id:"203178",title:"Dr.",name:"Lynda",surname:"Addou-Klouche",slug:"lynda-addou-klouche",fullName:"Lynda Addou-Klouche"}],corrections:null},{id:"56169",title:"The Role of Activating and Inhibitory NK Cell Receptors in Antitumor Immune Response",doi:"10.5772/intechopen.69729",slug:"the-role-of-activating-and-inhibitory-nk-cell-receptors-in-antitumor-immune-response",totalDownloads:2079,totalCrossrefCites:6,totalDimensionsCites:8,hasAltmetrics:0,abstract:"Natural killer (NK) cells express many newly identified activating and inhibitory receptors that upon engagement by cognate ligands on target tumor cells regulate NK cell antitumor activity. Recently, several paired NK cell receptor families that include receptors with similar binding specificities but opposite function have been defined. The expression of most important activating receptors, natural killer group 2D (NKG2D), natural cytotoxic receptors (NCR), DNAX accessory molecule-1 (DNAM1) and activating killer cell immunoglobulin-like receptors (KAR) is often decreased, while the expression of most prominent inhibitory NK cell receptors, killer cell inhibitory immunoglobulin-like receptors (KIR) and CD94/NKG2A, may occasionally be increased in malignancies. These data indicate that impaired NK cell antitumor response results from NK cell receptor alterations induced by suppressive factors in the tumor microenvironment, including cytokines, growth factors, enzymes and metabolites, as well as by chronic NK cell receptor engagement by the tumor. The established alterations in NK cell receptor expression in cancer patients represent potential disease biomarkers and may aid in choosing therapies that upregulate activating or block inhibitory receptor function. Accumulating knowledge of NK cell biology has been helpful in creating novel therapeutic approaches that by release from tumor-influenced immunosuppression potentiate NK cell activity in cancer patients.",signatures:"Gordana Konjević, Ana Vuletić, Katarina Mirjačić Martinović and\nRadan Džodić",downloadPdfUrl:"/chapter/pdf-download/56169",previewPdfUrl:"/chapter/pdf-preview/56169",authors:[{id:"143424",title:"Prof.",name:"Gordana",surname:"Konjevic",slug:"gordana-konjevic",fullName:"Gordana Konjevic"},{id:"203621",title:"Dr.",name:"Ana",surname:"Vuletic",slug:"ana-vuletic",fullName:"Ana Vuletic"},{id:"203622",title:"Dr.",name:"Katarina",surname:"Mirjacic Martinovic",slug:"katarina-mirjacic-martinovic",fullName:"Katarina Mirjacic Martinovic"},{id:"207134",title:"Prof.",name:"Radan",surname:"Dzodic",slug:"radan-dzodic",fullName:"Radan Dzodic"}],corrections:null},{id:"55518",title:"Clinical Applications of Natural Killer Cells",doi:"10.5772/intechopen.68991",slug:"clinical-applications-of-natural-killer-cells",totalDownloads:1998,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:0,abstract:"Natural killer (NK) cells are an essential component of the innate immune system, and they play a crucial role in immunity against malignancies. Recent advances in our understanding of NK cell biology have paved the way for new therapeutic strategies based on NK cells for the treatment of various cancers. In this section, we will focus on NK cell immunotherapy, including the enhancement of antibody‐dependent cellular cytotoxicity, the manipulation of receptor‐mediated activation, inclusion criteria based on killer cell immunoglobulin‐like receptor (KIR) ligand mismatches, and adoptive immunotherapy with ex vivo expanded chimeric antigen receptor (CAR)‐engineered or engager‐modified NK cells. In contrast to T lymphocytes, donor NK cells do not attack any recipient tissues based on allogeneic human leukocyte antigens (HLAs), suggesting that NK‐mediated antitumor effects may be achieved without the risk of graft‐versus‐host disease (GvHD). Despite reports of clinical efficacy, the application of NK cell immunotherapy is limited. Developing strategies for manipulating NK cell products, host factors, and tumor targets are thus current subjects of diligent study. Research into the biology of NK cells has indicated that NK cell immunotherapy has the potential to become the forefront of cancer immunotherapy in the coming years.",signatures:"Yui Harada, Koji Teraishi, Minori Ishii, Hiroshi Ban and Yoshikazu\nYonemitsu",downloadPdfUrl:"/chapter/pdf-download/55518",previewPdfUrl:"/chapter/pdf-preview/55518",authors:[{id:"203136",title:"Ph.D.",name:"Yui",surname:"Harada",slug:"yui-harada",fullName:"Yui Harada"},{id:"203138",title:"Mr.",name:"Hiroshi",surname:"Ban",slug:"hiroshi-ban",fullName:"Hiroshi Ban"},{id:"203139",title:"Prof.",name:"Yoshikazu",surname:"Yonemitsu",slug:"yoshikazu-yonemitsu",fullName:"Yoshikazu Yonemitsu"},{id:"203359",title:"Ms.",name:"Minori",surname:"Ishii",slug:"minori-ishii",fullName:"Minori Ishii"},{id:"203360",title:"Mr.",name:"Koji",surname:"Teraishi",slug:"koji-teraishi",fullName:"Koji Teraishi"}],corrections:null},{id:"55987",title:"Donor Natural Killer Cells and Their Therapeutic Potential in Allogeneic Hematopoietic Stem Cell Transplantation",doi:"10.5772/intechopen.69684",slug:"donor-natural-killer-cells-and-their-therapeutic-potential-in-allogeneic-hematopoietic-stem-cell-tra",totalDownloads:1324,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:1,abstract:"Natural killer (NK) cells were first identified and named for their “natural” cytotoxicity to reject bone-marrow allografts in lethally irradiated mice. Different from T cells, NK cells require no prior sensitization or immunization to lyse transformed or virally infected target cells and are non-major histocompatibility complex (MHC)–restricted. However, recent progress in understanding of NK cells biology has proved that NK cells share some similar characteristics with T cells. During development, NK cells also undergo “education” according to “missing self” principle, thereby become mature and acquire effector function. The discovery that NK cells are able to “remember” prior certain stimulations indicates they may also contribute to adaptive immunity. After hematopoietic stem cell transplantation (HSCT), NK cells are the first donor-derived lymphogenous cells to reconstitute and alloreactivitiy of donor-derived NK cells have been shown to mediate graft-versus-leukemia (GvL) effect rather than to induce graft-versus-host disease (GvHD). These properties make donor-derived NK cells appealing for applications to benefit the outcome of HSCT. Here, we will review the improved understanding of NK cell biology, discuss characteristics of donor-derived NK cells which are associated with beneficial outcome of HSCT and explore novel methodologies that enhance the therapeutic effect of donor NK cells.",signatures:"Bo Hu and Haiyan Liu",downloadPdfUrl:"/chapter/pdf-download/55987",previewPdfUrl:"/chapter/pdf-preview/55987",authors:[{id:"202281",title:"Dr.",name:"Haiyan",surname:"Liu",slug:"haiyan-liu",fullName:"Haiyan Liu"},{id:"202283",title:"Dr.",name:"Bo",surname:"Hu",slug:"bo-hu",fullName:"Bo Hu"}],corrections:null},{id:"56130",title:"Natural Killer Cells Interaction with Carbon Nanoparticles",doi:"10.5772/intechopen.69731",slug:"natural-killer-cells-interaction-with-carbon-nanoparticles",totalDownloads:1474,totalCrossrefCites:2,totalDimensionsCites:3,hasAltmetrics:0,abstract:"The increased use of nanomaterials for biomedical purposes has warranted the need to introspect their toxicological properties and assess their utility to human health, particularly the immune system. Natural killer (NK) cells hold a pivotal position in innate immunity and serve as first line of defense against foreign bodies. Acid functionalized Carbon nanotubes (CNTs) that easily polydisperse in aqueous solution and could be coupled with fluorescent molecules were used to study the effect of carbon nanoparticles on NK cells in vitro and in vivo. Flow cytometry-based assays were used to study the effect of CNTs on various physiological parameters of NK cells, such as cell recovery, apoptosis, cell cycle, and generation of reactive oxygen species. A downregulation of the cytotoxicity of IL-2-activated murine NK cells was observed in the presence of acid-functionalized CNTs. The mechanistic basis of this downregulation was studied by assessing markers of NK cell activation (CD69), generation (NLK1.1), degranulation (CD107a) and apoptosis (annexin V assay). This chapter provides a blueprint for assessing the effect of carbon nanoparticles on NK cells. The assays mentioned in this chapter can be extrapolated to study the effect of other nanoparticles on different cell types as well.",signatures:"Anwar Alam and Rajiv K Saxena",downloadPdfUrl:"/chapter/pdf-download/56130",previewPdfUrl:"/chapter/pdf-preview/56130",authors:[{id:"202626",title:"Prof.",name:"Rajiv",surname:"Saxena",slug:"rajiv-saxena",fullName:"Rajiv Saxena"}],corrections:null},{id:"57507",title:"A New Method to Determine Natural Killer Cell Activity Without Target Cells",doi:"10.5772/intechopen.71912",slug:"a-new-method-to-determine-natural-killer-cell-activity-without-target-cells",totalDownloads:2264,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:1,abstract:"Natural killer (NK) cell activity is a conventional parameter used to determine the performance lytic activity against tumor as well as virus-infected cells in innate immunity. However, use of this parameter has several problems related to bioassay measurements. To measure NK cell activity, target cells and cell culture equipment are required and adequate pre-culture of target cells is needed to maintain constant sensitivity for NK cells. NK cell-activating receptors play an important role in the recognition of targets, which transduce the signals necessary for cellular machinery to induce target injury and cytokine production. We statistically examined the parameters related to the NK cell activity of human peripheral blood mononuclear cells (PBMCs) by multiple regression analysis, and obtained a formula with NK cell % and RNA levels of two genes in isolated NK cells. The score calculated using this formula with the three measured values showed significant correlation with NK cell activity. This prediction score, named the non-incubating natural killer (NINK) score, which is independent of target cells, is not affected by inappropriate preparation of those targets, and allows us to accurately compare the performance of NK cell activity among specimens.",signatures:"Yasumitsu Nishimura, Naoko Kumagai-Takei, Suni Lee, Hidenori\nMatsuzaki, Kei Yoshiotme and Takemi Otsuki",downloadPdfUrl:"/chapter/pdf-download/57507",previewPdfUrl:"/chapter/pdf-preview/57507",authors:[{id:"34101",title:"Prof.",name:"Takemi",surname:"Otsuki",slug:"takemi-otsuki",fullName:"Takemi Otsuki"},{id:"48627",title:"Dr.",name:"Naoko",surname:"Kumagai-Takei",slug:"naoko-kumagai-takei",fullName:"Naoko Kumagai-Takei"},{id:"48631",title:"Dr.",name:"Yasumitsu",surname:"Nishimura",slug:"yasumitsu-nishimura",fullName:"Yasumitsu Nishimura"},{id:"104893",title:"Dr.",name:"Suni",surname:"Lee",slug:"suni-lee",fullName:"Suni Lee"},{id:"104894",title:"Dr.",name:"Hidenori",surname:"Matsuzaki",slug:"hidenori-matsuzaki",fullName:"Hidenori Matsuzaki"},{id:"219725",title:"Dr.",name:"Kei",surname:"Yoshitome",slug:"kei-yoshitome",fullName:"Kei Yoshitome"}],corrections:null}],productType:{id:"1",title:"Edited Volume",chapterContentType:"chapter",authoredCaption:"Edited by"},subseries:null,tags:null},relatedBooks:[{type:"book",id:"5467",title:"Immunopathogenesis and Immune-based Therapy for Selected Autoimmune Disorders",subtitle:null,isOpenForSubmission:!1,hash:"c7843c501b6842ae6f0f150bfd46370d",slug:"immunopathogenesis-and-immune-based-therapy-for-selected-autoimmune-disorders",bookSignature:"Mourad Aribi",coverURL:"https://cdn.intechopen.com/books/images_new/5467.jpg",editedByType:"Edited by",editors:[{id:"40046",title:"Prof.",name:"Mourad",surname:"Aribi",slug:"mourad-aribi",fullName:"Mourad 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Modifications in mechanism occurring at the morphological, anatomical, and physiological level are regulated by the capacity of a plant to adjust to abiotic and biotic stresses [1, 2, 3, 4]. The resulting survival response and survival capacity may vary depending on plant life stages [1, 2, 3, 4]. Plasticity mechanisms discovered in plants are like those described in animals and humans, illustrating the conserved connection between environmental selection and adaptive response [2, 3, 5, 6, 7, 8, 9, 10, 11]. Research into the connection between environmental stress, environmental selection, and plant plasticity has also identified both general and unique plasticity mechanisms that differ between wild, i.e., non-cultivated, and cultivated plant species [1, 12, 13, 14, 15]. However, a review analyzing the contribution of key traits responsible for varied plasticity mechanisms in wild and cultivated plants has not occurred. Thus, the range of plasticity occurring in wild plants will be compared with plasticity mechanisms in cultivated plants. Similarities and differences in plasticity responses will be highlighted between the two groups, with a specific focus on climate imposed global abiotic stresses like drought [14].
All plants have evolved unique life cycle characteristics that enhance survival and adaptation to diverse short and long-term climatic events that limit resources. Phenotypic responses occur at every stage of plant development, and influence overall plasticity from one generation to the next. Understanding and tracking phenotypic plasticity of wild plants in cultivated plants first requires defining biological reaction norms and their alternatives to clearly illustrate the differences between biological plasticity and non-plastic responses. Examples of phenotypic responses include: (1) rapid seedling growth (2) a short vegetative phase, (3) deep root systems, (4) high seed output, (5) discontinuous or extensive seed dormancy, (6) efficient cellular defense machinery, and (7) environmental plasticity. Although all plants exhibit phenotypic responses, the level of response is largely influenced by the degree of cultivation. Several species of trees and weeds are exceptional models for defining and tracking the range of both short and long-term heritable characteristics of wild plasticity [1, 4, 12, 16, 17, 18, 19, 20, 21]. Drought response studies in agronomically important, and highly cultivated crops like wheat, add perspective about the contributions of selective breeding programs; how increased cultivation results in gains or losses in adaptive responses and plasticity [7]. Transitional plant models, such as
Climatic events trigger heterogeneous responses in plants. Plant responses occurring from biotic or abiotic factors drive two distinct adaptation mechanisms, natural selection and phenotypic plasticity. Both mechanisms reveal the full genetic capacity of plants [22, 23]. The genetic makeup or genotype of each plant species determines how a plant will react in new environments [24]. Accumulated exposure to novel environmental stresses over many generations may increase selection toward the frequency of favorable alleles versus a reduction of unfavorable alleles, and results in less genetic diversity [22]. Otherwise, in natural selection, any change in plant phenotype is defined as phenotypic plasticity [25]. Changes in phenotypic plasticity impact individual fitness without changing genetic diversity [22, 26]. Sometimes a novel genotypic response does not deviate from a normal range of reactions, i.e., the reaction norm, and sometimes it does [27]. Thus, plants have a wide array of genotypic responses that impact phenotype. Non-cultivated plant species like trees acquired wild plasticity through the combination of both the long-term accumulation of genetic changes and the conservation of favorable survival strategies through time [24]. Adaptive responses result in phenotypic plasticity [22, 26]. Adaptive responses also maximize phenotypic fitness, or the ability to respond and survive in changing environments [27]. Breeding programs have accelerated the adaptive process to abiotic stresses, like drought, in domesticated plant species by selecting for tolerance to drought or increased resource-use efficiency [28]. This approach has allowed breeders to select for favorable plant responses based on flexibility to varied environmental changes. A broad understanding of wild plasticity in non-domesticated plant species will enhance and extend our current understanding of the range of plasticity mechanisms in cultivated plants [2, 3, 5, 6, 7, 8, 9, 10, 11].
All terrestrial plants are stationary and adjust phenotypic responses to survive in fluctuating environments [22, 26]. A wide spectrum of adaptive variation occurs with a specific phenotypic response, and which is defined as phenotypic plasticity [14]. Three recognizable outcomes associated with a phenotypic response, as illustrated in Figure 1, are: (1) a neutral response, (2) an adaptive response, or (3) a maladaptive response [13, 22, 27]. Each panel illustrates the relationship between a phenotypic response and a change in environment. Red, green, or blue colored lines represent different genotypes or individuals [13, 22, 27].
Recognition of the different reaction norms. The three major responses; neutral, adaptive, and maladaptive, which occur within the plasticity spectrum [
A neutral response occurs when there is no observable change in plant fitness or plasticity after exposure to novel environmental stress (Figure 1a). Canalisation and developmental stability are components of neutral responses that create some confusion in understanding and mapping phenotypes [29]. Canalisation describes the occurrence of a constant phenotype in a given population that is not influenced by environmental or genetic regulation [29]. Developmental stability describes the degree to which organisms withstand environmental changes or genetic perturbations during development [29]. Canalisation measures gene rigidity or the resistance of genes to altered function during environmental changes [29, 30]. Canalisation is a useful measure of genetic robustness and is more frequently described than adaptive plasticity in plants [29, 30].
Adaptive responses occur in new environments and may or may not occur as a direct result of genetic variation [29]. Adaptive responses result in beneficial changes that maximize phenotypic fitness (Figure 1b–d) [27]. Not all phenotypic changes occur because of beneficial adaptive responses [27, 29, 30]. Individuals within a population may experience random passive phenotypic changes that are limited to specific phenotypic traits or that act more broadly impacting adaptive performance at all stages of plant development [29, 30]. Plasticity may be controlled by a single gene or many genes [31, 32]. The plasticity threshold of a plant is a function of individual, pleiotropic, and collective responses within a population. This mosaic of responses influences genotypic selection [33, 34].
Not all adaptive strategies are beneficial for plants and often result in decreased fitness or yield [35]. A maladaptive response describes a phenomenon which reflects the absence of plasticity (Figure 1e) [34]. Maladaptive responses are not easy to distinguish from neutral responses because the average response of the population may mask any decline in response by individuals within the population over a long period of time [35]. Maladaptive responses are often misinterpreted as adaptive responses and difficult to study genetically [34, 35].
All phenotypic responses, neutral, positive, and negative, may occur simultaneously within an individual or across a population (Figure 1f) [13]. Changes in plasticity may be measured by examining the relationship between a specific genotype (G) in a specific environment (E) [13]. A genotype-by-environment (GXE) study tracks genetic plasticity and is a powerful tool for targeted genotypic selection [13, 33, 34].
Phenotypic plasticity, especially within wild plant populations, is a mechanism that enhances plant invasion and survival [12]. The invasiveness of a plant species is influenced by many phenotypic characteristics and responses [12]. The three major phenotypic characteristics that impact plasticity in wild plant populations are plant development, plant morphology, and plant physiology (Figure 2) [36]. Phenotypic responses associated with each characteristic occur at every stage of plant development, influencing the overall plasticity from generation to generation (Figure 2). Common phenotypic responses known to be associated with plant development, plant morphology, and plant physiology include: (1) rapid seedling growth allowing maximum capture of light, water, and nutrients [37, 38, 39, 40, 41], (2) a short vegetative phase allowing life cycle completion in various growing seasons and conditions [42, 43, 44, 45, 46, 47], (3) deep root systems allowing plants to survive through drought conditions [47, 48], (4) high seed output ensuring spatial and temporal dispersal, (5) discontinuous or extensive seed dormancy ensuring germination only in favorable conditions [49, 50, 51], (6) efficient cellular machinery for scavenging reactive oxygen species (ROS) [52, 53], and (7) environmental plasticity, or the ability to respond to changing biotic or abiotic environmental factors [1, 13].
The key characteristics and responses of wild plant plasticity including plant development (green), plant morphology (yellow), and plant physiology (blue) [
Phenotypic plasticity was first described for non-cultivated plants species including trees and weeds [1, 4, 12, 17, 18, 19, 20, 54]. Trees are excellent models for studying phenotypic plasticity due to their longevity [12]. Trees have developed a diverse set of plasticity mechanisms that are specific for both short and long development programs occurring in different developmental tissues at the same time [12]. Simultaneous root and leaf canopy development are an example of parallel programing [12, 54]. Phenotypic plasticity in trees occurs through a diverse collection of physiological, anatomical, and morphological responses [12, 54]. Many studies exploring global warming have investigated the possibility of using physiological or morphological indicators of beneficial adaptive responses as predictors of species survival [1]. Adaptive mechanisms in trees, as well as other plants, are important for mitigating the stress that is associated with fluctuations in native environments or, after new colonization, for rapid adaptation to novel environments [54, 55, 56, 57]. Studies investigating drought stress in trees have shown that by reducing the leaf canopy and increasing root proliferation, trees become more drought tolerant because both phenotypic responses limit water loss [58]. The occurrence of phenotypic responses occurring in parallel suggests that there may be a coordinated regulation of these traits [59, 60]. Other traits indicative of drought responses and plasticity in trees include leaf area, leaf dry mass, leaf mass per area (LMA), leaf tissue density, net photosynthesis, stomatal conductance, leaf respiration, water use efficiency, leaf water potential at midday, total chlorophyll content, relative water content, gross photosynthesis, leaf transpiration, and the ratio between leaf respiration and net photosynthesis [58]. Drought avoidance may also be viewed as a strategy for drought tolerance by altering the timing of growth and reproduction [14]. By maximizing the adaptive response of traits related to drought response, the overall fitness of an existing population of trees has the potential to adapt to a new environment [58]. However, if a given climatic event exceeds the limit of adaptive capacity, the same population of trees may also be replaced by a new, more adapted species [14].
Plasticity in weeds, as with trees, is governed by adaptive responses that impact physiology, morphology, and anatomy [36]. However, unlike trees, many weed species have relatively short life spans and must make rapid and frequent adjustments to environmental changes to ensure survival [16]. In addition to the wild characteristics for plasticity listed above, other characteristics in weeds that demonstrate enhanced phenotypic plasticity include: discontinuous or extensive seed dormancy ensuring germination only in favorable conditions, indeterminant or simultaneous flowering and vegetative growth, self-compatibility allowing genetic divergence from previous generations without requiring special pollinators to ensure seed viability, long-distance seed dispersal by air or water; competition with crop plants resulting in reduced crop yield, sexual and asexual reproduction strategies; and allelopathy, or the ability to produce chemicals that retard or kill other plants (Figure 2) [16, 36, 61]. Adaptive responses in weeds occur throughout development [16, 36]. Sometimes adaptive responses are more apparent in plant architecture than in signaling responses, are more pronounced at certain developmental stages or in specific populations, or involve the same tissue types during different developmental phases [1, 16, 36, 61]. The invasiveness of weeds is thought to be associated with several phenotypic plasticity traits including plant height, flower development, flowering, and light quality, [62, 63]. A direct correlation between plant height and invasiveness remains unclear. However, there may be an association between tall plant phenotypes, increased phenotypic diversity, and higher plant abundance in unfavorable environments [63]. Associations have not been observed with flowering phenology among native and non-native plant populations, but this may be because flowering time is dependent on the environment [62, 63, 64]. Flower development and invasiveness in Purple loosestrife (
There is not enough data about the genes, promoters, and regulatory elements that control “invasive” or “weedy” phenotypes commonly observed in wild plant populations. However, the phenotypes provide key insights into potential gene families and signaling pathways. Adaptive phenotypes also provide evidence that plasticity responses are controlled genetically and by specific plasticity genes [6]. The accumulation of genetic modifications associated with adaptive responses can be tracked through time and are genetically controlled [6]. Two models have been proposed to explore how changes in adaptive response occur. The first model proposes that the expression of structural genes varies as the environment changes [68]. Genetic plasticity is not regulated by plasticity genes, rather by changes in gene expression of structural genes resulting in phenotypic changes or plasticity [68]. The second model proposes that specific regulatory genes, i.e., plasticity genes mediate responses for structural genes [69, 70]. The resulting change in expression of the regulatory genes in response to environmental changes is what ultimately controls the pattern of plasticity [69, 70].
There are four primary mechanisms in wild plant populations that regulate plasticity through adaptive responses [6]. The four plasticity mechanisms are physiological, developmental, cellular, and epigenetic responses [6]. Physiological plasticity describes all physiological responses associated with phenotypic traits and signaling networks [40, 71]. Developmental plasticity is associated with human or animal neural developmental, and plant embryonic development, in response to stress [6, 40]. Cellular plasticity describes adaptive responses within cells that are often associated with reducing reactive oxygen species accumulation through redox mechanisms [72]. Epigenetic plasticity describes changes to molecular mechanisms in response to abiotic stresses resulting in altered gene expression and function without changes in the DNA [71].
Physiological plasticity is the most dynamic of plasticity mechanisms and is often involved in all other mechanisms of plasticity [40, 71]. Novel and emerging environments trigger many physiological responses such as carbon dioxide (CO2) assimilation, changes in chlorophyll content, water use efficiency, sugar sensing and photosynthesis [73]. Physiological changes correlate directly to plant fitness, and changes in plasticity determine how a plant responds to environmental stresses [73, 74]. Studying the association between a physiological phenotype and changes in gene expression within wild populations will make it is possible to identify and target genes that are responsible for adaptive responses, i.e., plasticity genes [24, 73, 74]. In this way plasticity genes and gene variants become a selective tool for understanding plasticity heritability dynamics, as well as identifying positively adapted populations [24, 73, 74, 75].
Seed dormancy is an excellent example of physiological plasticity [73, 74] Seed dormancy prevents germination out of season, even under favorable conditions, and ensures species survival of natural catastrophes [16, 76]. Environmental cues such as light, temperature, and moisture impact the depth of seed dormancy and the length of time required for dormancy release [76]. In weeds, discontinuous or extensive seed dormancy ensures germination only in favorable conditions and confers environmental plasticity, or the ability to respond to changing biotic or abiotic environmental factors [16].
Discontinuous or extensive seed dormancy impacts environmental plasticity through variable emergence timing throughout a growing season [76]. Discontinuous seed dormancy is likely a major “weedy” characteristic contributing to physiological plasticity in many wild plants and weed populations [76]. Downy brome (
There is currently very little information about the specific genes or molecular mechanisms regulating dormancy or dormancy loss in many weeds or wild plant species [77]. Gaps in molecular information slow the progress for understanding the impact of wild plasticity on adaptability [1, 16]. However, detailed physiological observations and translational research are useful tools. These are powerful tools for studying the mechanisms that drive physiological plasticity in the seed and throughout all plant life stages, in natural and agricultural environments, and in both wild and cultivated plant populations [1, 16, 82, 83, 84, 85, 86].
Basic research has established that a seed’s transition from dormancy to germination is controlled by the plant hormones, abscisic acid (ABA) and gibberellin (GA) [81, 82]. ABA establishes seed dormancy during embryo maturation and maintains dormancy in mature seeds, whereas GA stimulates seed germination [34, 36]. Dormancy studies in model systems including
Developmental plasticity was first identified in, and is most often associated with, human and animal development [40]. Developmental plasticity refers to the impact of environmental stimuli on embryonic development [6]. Within the plant biology community, there remains some skepticism surrounding the existence of plant developmental plasticity mechanisms, and how to best identify and characterize them [5, 6, 7]. Despite these challenges, recent paradigm shifts in conventional thought have resulted in significant efforts toward studying the impact of developmental plasticity in cultivated plant species [5, 6, 7, 40, 72].
Developmental plasticity directly impacts phenotypic plasticity and is characterized using GXE experiments that investigate the interactions of genotype in a given environment [7, 101, 102, 103, 104]. Developmental plasticity occurs commonly within plant populations when a given population inhabits moderate environments [2, 18]. Abiotic stresses, like drought, trigger physiological and developmental plasticity in plants [7]. The degree of developmental plasticity observed in plants resulting from abiotic stress is directly connected to a plant’s development phase [7]. Some phases of development are more responsive to environmental changes and display a more plastic response than others [7]. It was found in spring wheat that the early developmental stages tillering and heading (after spike formation) show more morphological and physiological plasticity than other developmental phases [7]. Cold tolerance in quinoa is also based on developmental plasticity, and associated with grain formation [105, 106]. Flowering time is another trait associated with developmental plasticity across plant species [6]. A shift in flowering time in response to drought allows for accelerated seed set, thus ensuring species survival, even in non-ideal growing conditions [6].
Plant cellular plasticity allows cells to respond to the negative impacts of biotic and abiotic stresses. Cellular plasticity occurs through long-range signaling via hydraulic, electrical, and chemical signaling mechanisms [107]. One example of chemical signaling directly connected with plant cellular plasticity occurs when plants experience oxidative stress. Environmental stresses stimulate the production of toxic chemicals known as reactive oxygen species (ROS) [108]. The function of scavenging enzymes is to quench the flux of ROS [108, 109, 110, 111, 112, 113, 114]. When ROS levels are elevated due to environmental stress, the activity of scavenging enzymes, including ascorbate peroxidase, superoxide dismutase (SOD), and catalase (CAT) increases [108, 109, 110, 111, 112, 113, 114].
Cellular plasticity is a very dynamic process whereby ROS scavengers are acting simultaneously in different cellular compartments including the cell wall membrane, cytoplasm, chloroplast, mitochondria, peroxisomes, and the apoplast [115, 116, 117]. The peroxisomes are the most important indicators of environmental stress, ROS-scavenger activity, and cellular plasticity [115]. Peroxisomes proliferate in response to an array of environmental stresses including light, ozone, metal, and salt [119]. Peroxisome number may fluctuate depending on cultivar or genotype [118, 119, 120, 121, 122]. An emerging hypothesis about cellular plasticity is that relative peroxisome abundance may be a good predictor for cellular plasticity mechanisms [123, 124]. Peroxisomal proliferation occurs because of environmental stress, and, any change in a phenological trait occurring from a change in environment is defined as cellular plasticity [123, 124]. Investigations of peroxisome proliferation in response to drought tolerance demonstrate that peroxisome abundance is correlated with abiotic stress response and impacts GXE interactions [123, 124]. A negative correlation also exists between peroxisome abundance and several phenological traits including plant biomass, root dry weight, and grain yield [123, 124]. Therefore, peroxisome abundance is an emerging tool for measuring cellular plasticity mechanisms of adaptation, and ROS homeostasis [123, 124].
Plasticity responses exist as both the inherent genetic machinery (past regulatory events), and as part of regulation occurring outside of the genetic code (epigenetically) [71]. Epigenetic mechanisms include DNA methylation, non-coding RNA, chromatin remodeling, and histone modifications [71]. Changes in the environment trigger heritable changes in gene expression which result in stable phenotypes [71]. DNA methylation is the most common, and perhaps best understood mechanisms controlling epigenetic plasticity in plants [71]. Studies using Arabidopsis epigenetic recombinant inbred lines (epiRILS), i.e., lines with nearly identical genomes but contrasting DNA methylation patterns, demonstrated that plasticity to water availability and nutrient loss is controlled through changes in DNA methylation [80]. Epigenetic changes rather than genetic changes contribute to changes impacting phenotypic plasticity [71]. Other research has demonstrated that epigenetic regulation impacts heritability in specific phenological traits like plant height, plant biomass, seed/fruit production, the root-to-shoot ratio, and flowering time [71, 125, 126, 127]. Heritable traits are very important in breeding programs, and the role of epigenetics in regulating these traits is now only being characterized and understood [128].
Decreased genetic diversity in plants populations is often associated with increased cultivation [7, 129]. Less cultivated plant populations tend to have more genetic diversity or “wildness” than plants that have been domesticated [129]. Wild characteristics broaden genetic responses and are valuable for maintaining phenotypic plasticity [129, 130, 131]. Leveraging broad genetic responses to enhance plasticity is especially important for the survival of plant species in unpredictable and changing climates [74, 75].
Since the dawn of agriculture, farmers have used selective breeding techniques for cultivating and domesticating wild plants for food [132]. Seeds from wild plant populations are smaller, an adaptation thought to enhance dispersal [132]. From an agricultural perspective, increased domestication is useful for reliable germination, uniform emergence, uniform stand establishment, larger seed size, increased yield, and improved nutrition [132]. Domestication of wild maize, soybean, and barley has resulted in significant increases in seed size [86]. However, there has also been a negative cost associated with domestication [86]. In maize, soybean, and rice, domestication and intensive cultivation have resulted in the elimination of genetic loci in modern crop cultivars [86, 133, 134, 135, 136]. Breeding strategies that do not address adaptation and plasticity decrease trait diversity and may limit the development of new crop varieties with the ability to adapt to insects and extreme environmental fluctuations [133, 134, 135, 136].
A reduction in heritability of favorable traits within breeding populations has been one of the main reasons plant breeders have explored the possibility of integrating genetic diversity from wild populations (landraces) back into selective breeding programs [133, 134, 135, 136, 137]. Two wild plant models that have been very instrumental in the effort to introduce diversity back into breeding population are: (1) barley (
Barley was domesticated very early in history from the wild grass relative,
Quinoa, like barley, was recognized as a valuable food resource, and was domesticated very long ago [144]. Although quinoa has been highly domesticated, it retains vast genetic variability and plasticity with a wide range of resistance to many abiotic and biotic stresses [144, 145]. Quinoa thrives in extreme environmental conditions including in regions with high salinity soils, areas of extremely low precipitation, and environments with extremely cold temperatures [105, 146]. Moreover, quinoa grain is resistant to starch degradation in environments susceptible to extreme temperature and moisture fluctuations [147]. The differences in plasticity discovered between wild and domesticated quinoa species illustrate the importance of continued studies identifying physiological and genetic mechanisms regulating plasticity [147]. These discoveries also highlight the feasibility and importance of selectively breeding for gene targets that improve adaptability and fitness [133, 134, 135, 136]. Additionally, because quinoa is a polyploid, it is a rich resource for studying how complex genomes contribute new dimensions of genetic regulation to phenological plasticity [147]. Recent studies investigating modern cultivated varieties of quinoa show that cellular plasticity mechanisms, and more specifically ROS homeostasis, are dependent on both genotype and type of stress [123]. The emerging discoveries in quinoa are important because they provide a model for how plasticity mechanisms present in other polyploid crop species may be regulated [123].
The discovery and utilization of improved traits that enhance the adaptability of crops to increasingly variable environments will help to ensure long-term crop stability in changing climates [74, 128, 129]. Knowledge of phenological plasticity in wild populations will continue to benefit breeding programs [28]. Although wild genomes increase genetic complexity and may impact plasticity and fitness in unpredictable ways through changes in development, morphology, or physiology, one of the discovered benefits of increased diversity is increased adaptability [71, 129]. Over the last decade, advancements in genetics, molecular biology, systems biology, and statistical modeling have removed many of the barriers for understanding the regulation of complex plasticity networks in plants [13]. Association mapping, next generation sequencing, and genotype-by-phenotype (GWAS) approaches have greatly improved our comprehensive understanding of plasticity and the impacts of genomic selection [141, 142, 143]. Additionally, translational approaches utilizing a wealth of genomic information from both model plant systems and non-domesticated relatives have provided a framework for parallel studies in a wide range of plant populations. These studies have helped to uncover the developmental, cellular, and epigenetic mechanisms that regulate plasticity in all plants [6, 13, 71, 74, 142, 143].
One of the benefits of increasing genetic diversity in domesticated populations, from a long-term agricultural perspective, is the increased likelihood of plant population survival in unpredictable environments. In the past, evaluating the contributions of specific traits on phenological plasticity in plants was challenging due to experimental limitations and gaps in knowledge. However, emerging research continues to be extended from model systems directly to wild and cultivated plant populations to uncover the full potential of plasticity. New areas of research will need to investigate plasticity using a systems biology approach. Work should continue to explore the degree of conservation of plasticity existing between monocots and dicot crops, as well as comparing the contributions of ploidy on diversity. Other areas of research should address how DNA methylation and epigenetic mechanisms contribute to plant plasticity and may be fully utilized in plant improvement programs. Additional work should focus on how the simultaneous deployment of multiple plasticity mechanisms during plant developmental shift in changing environments using newly identified plasticity markers like the peroxisomes. Continued plasticity research will be is critical for understanding how to maximize the benefits of both domestication and wild genetic diversity to maximize adaptation and fitness in a new area of climate diversity.
In the late summer of 2018, the Hambacher Forst (Hambach Forest) in Germany appeared prevalently in the media covering the strong protests against the intention of the utility company Rheinisch-Westfälisches Elektrizitätswerk AG (RWE) to grub large parts of the remaining forest in order to mine the lignite underneath. Up to 50,000 people from across Germany as well as neighboring countries gathered for protest marches in order to save the forest and express their position against lignite mining and to demand more political action regarding climate protection. The grubbing was suspended when in October 2018 the Higher Regional Court of Munster issued a provisional stop until there was going to be a decision as to whether the Hambach Forest falls into a category of the Habitats Directive.1 This was an option since the forest is habitat to 13 species considered in the Directive, among them the Bechstein’s bat (
Several factors seemed to be of relevance for the massive protests and the unexpected, high commitment of the population, either as participants in rallies or as debaters in social networks or the like. First, the forest on its own as an old forest and as a habitat for endangered species might be seen as valuable and irreplaceable [4]. Second, worries about climate change have gained in importance and were fostered not least by the extremely hot summer of 2018, and the increasing awareness that coal-fired power generation is among the largest sources of carbon emissions in Germany. Third, for many people, RWE turned into an enemy image, as the company has been made responsible not only for massive carbon emissions, but also for the destruction of nature and villages, despite the efforts of RWE to compensate relocated people and to re-cultivate large areas. This position, however, neglects proprietary rights, which RWE holds based on the acquisition of the Hambach Forest in 1978, operating permits, and mining rights, all negotiated with the provincial government in Dusseldorf, represented by different parties (Social Democrats, Christian Democratic Union, and Green Party). Since 1978, the size of the Hambach Forest has shrunk from 4100 ha to only about 500 ha in 2020, and since 2012, the Hambach Forest has been occupied by about 20–100 people permanently living there in self-constructed tree houses. However, the ownership based on the legal definition may be in contrast to what people perceive as legacy or moral ownership here [5]. The Hambach Forest eventually became a symbolic battleground for climate activists from Germany and other countries. Ten thousands of people have visited the Forest since, and its publicity goes well beyond the borders of Germany [4, 6, 7].
Accordingly, the Hambach Forest has become a location of “meaning,” and this meaning can be attributed on vastly different scales. Such “meaning” does not manifest itself in particular physical characteristics, but is instead attributed by humans and may be closely linked to notions of identity and sense of “belonging” [5]. Only places identified as symbolic by a certain number of individuals are socially recognized as such, and a group can form and give itself an identity within this movement of recognition [8]. Most generally, a place can be considered “symbolic” whenever it contributes significantly to giving a group an identity—for example, the stadium of “their” club is something meaningful for football fans. Members of a particular scene are aware of this, and the symbolic meaning of a place is common understanding among them. Accordingly, the symbolic character of a location is both, a powerful matter and a power instrument: the person who manipulates symbols can also manipulate processes of identification and thus take an influence on the constitution of the group [8]. Further, a symbolic place does not have the same meaning seen from nearby or from a distance, by a small group or by a large community, from inside or from outside, by “us” or by “others,” and through time [8]. This symbolic aspect may partly explain the fierce fight over the Hambach Forest, since the topic activates the identification with either one side: following traditional rules or claiming change in order to protect nature and climate.
Against this background and given the described unusually high empathy for the forest, the question about its value for the German population arose. We therefore intended to find out whether it was possible to measure the meaning of the forest in the view of the population and to translate it into quantifiable values in order to make it comparable. These values are to represent its role in the controversial political debate on climate protection, transformation strategies, and coal phase-out in Germany. It thus may indicate the non-use and probably symbolic value of the Hambach Forest. Furthermore, stated values can also be considered as an indicator of how important the protection of the forest for single individuals is. Since no similar case is known to us so far, this study has a rather explorative character.
The structure of the paper is as follows: In section 2, we provide a literature review about valuation studies of forests. Methods and procedure are described in detail in section 3, followed by the results in section 4. This paper ends with a discussion and conclusion section.
In order to elucidate the values of environmental goods, several methods have been developed depending on the values to be considered. Although the importance of environmental goods to humankind has many dimensions (e.g., ecological, sociocultural, or economic), the values are usually expressed in monetary units as an important tool to raise awareness and convey the (relative) importance of ecosystems and biodiversity to policymakers [9]. Economists have recognized the possibility that individuals who make no active use of a particular forest, river, certain species, or other such natural resources may, nevertheless, derive satisfaction from their mere existence, even if they never intend to make active use of them [10, 11, 12, 13, 14, 15, 16]. This concept has come to be known as “existence value,” and it is the major element of what is now referred to as “non-use” or “passive-use” values [17]. The most common methods for the evaluation of environmental goods, which comprise also non-use values, are direct methods such as the contingent valuation method (CVM) or Choice Experiments (CE). As part of these methods, individuals are presented a hypothetical scenario for which they are asked to state their willingness to pay (WTP) and/or their preferences for a change in the provision of a specific environmental good [18].
Many surveys have been carried out during the last four decades about values of sylvan ecosystems and their ecological services. However, the WTP values are hardly transferable due to several reasons: First, they are scenario-dependent. Second, WTP values normally depend on individual characteristics, such as attitudes and sociodemographic variables. Third, the values may change quite a bit over time according to circumstances [19]: for example, about 40 years ago, there were hardly any protests against the cutting of the Hambach Forest, because, on the one hand, there was still a large part of the forest remaining, and on the other hand, climate change and the impact of coal-fired power generation were almost unknown, at least for large parts of the population. Fourth, by conducting a survey, previously unknown and/or unexpected correlations may be revealed. Nevertheless, procedures and results of comparable studies are useful for the design and the interpretation of new surveys.
In a first step, we analyzed a database of more than 80 surveys about preferences for wooden areas applying CVM, CE, travel-cost method (TCM), or benefit transfer method (BTM) within German-speaking countries during the last three decades [20]. Most of the studies measure recreational values by directly asking for the WTP for entrance fees [21, 22, 23, 24, 25], or they evaluate minor changes in attributes such as the introduction of environmental protection programs by asking for additional taxes or the like [26, 27, 28]. None of the studies deal with pure existence values only, and thus, no directly comparable values could be extracted from the studies listed in the database.
In a second step, we searched the Environmental Valuation Reference Inventory (EVRI)2 database, which compiles environmental valuation studies from all over the world, for studies about values of woods and forests in order to find comparable studies to the case of the Hambach Forest. As search criteria, we chose “plants,” since this comprised both forests and woodlands, “willingness to pay,” “passive uses,” and “stated preference” or “simulated market price” in order to identify comparable studies. Altogether, 182 studies were found (January 2020), of which 94 indicated “forest” as environmental asset, 88 “trees,” 50 “woodland,” and 16 “rainforest.” Since some studies consider more than one environmental asset, overlaps occurred. After deleting those, 171 studies remained. Most of them address preferences for specific aspects such as species diversity, infrastructure, preferences for leisure activities, or forest protection schemes. In most of the studies on rain forests, the researchers surveyed the willingness to pay for the preservation of a certain minimum area. Only five studies dealt with the total value of a forest rather than values for single characteristics.
The first study in chronological order was a cost-benefit analysis about the option to log the Aorangi-Awarua-Forest in New Zealand (Table 1). A CV among 500 New Zealanders was conducted via mail in 1991 by Beanland [30] in order to find out whether the total economic value of the forest was higher than the revenues from logging it. The mean WTP to preserve the forest was 13.12 New Zealand $ as a yearly payment, with 41% of the respondents willing to pay at all. This amount is comparable to roughly 10€ currently when accounting for exchange rates and inflation. However, since in this New Zealand mail survey, the return rate of questionnaires was just around 50%, and normally those who are less interested in the topic are more likely not to send back the questionnaire [35], an interpolation of the mean WTP to the total population did not appear advisable.
1 | 2 | 3 | 4 | 5 | |
---|---|---|---|---|---|
Beanland [30] | Kniivilä et al. [31] | Amirnejad et al. [32] | Veisten and Navrud [33] | Broberg [34] | |
Survey year | 1991 | 1999 | 2004 | 1995 | 2005 |
Country | New Zealand | Finland | Iran | Norway | Sweden |
Method | Mail survey | Mail survey | Personal interview | Mail survey | Mail survey |
Selected sample | 500 | 800 | n.a. | 2,498 | 2,000 |
Participation rate | 50% | 59% | n.a. | 71% | 49% |
Sample size | 225 | 472 | 950 | 1776 | 930 |
WTP method | Open ended | DC | DC | DC/open ended | Open ended |
% pos. WTP | 41% | 36.5% | 65% | 25–39% | 45% |
WTP value | 10€ | 65€ | 40€ | 27–61€ | 35€ |
Forest size | 5142 ha | 20,000 ha | 1,900,000 ha | n.a. | 126,000 ha |
WTP surveys about forest areas with mainly non-use values.
Source: own compilation.
The second study by Kniivilä et al. [31] assessed the regional and local user and non-user benefits of the current conservation of old forests in the region of Ilomantsi/Finland in 1999 by surveying 800 people in North Karelia. The response rate was 59.2%, the median WTP was 19€, and the mean WTP 48.6€ per person/year, which corresponds to 25€ and 65€, respectively, in 2019. The WTP values were taken by the dichotomous choice (DC) question format, which normally leads to higher WTP values [33]. However, 18.5% of the respondents chose an “I don’t know” option when they were asked whether they would be willing to pay a certain amount for the preservation of the forest and were excluded from further analysis. About 45% of the remainder had a true zero WTP. Indeed, recreational values of the evaluated forests there are non-negligible, since the forests are popular tourist destinations [31].
Amirnejad et al. [32] conducted a CV in order to estimate the existence value of north forests in Iran. By analyzing the answers from personal interviews of about 950 residents of Iran, the mean WTP for the protection of the forests was 30.12 US$ annually (corresponding to roughly 40€ in 2020), which is quite high considering that the GDP per capita in Iran in 2004, when the interviews for this survey were conducted, was only 2500 US$. However, the WTP values appear more valid when considering that the sample is highly biased in terms of education and income. The rate of respondents with a positive WTP is indicated with 65%, of whom 80% have already visited the north forests of Iran. The rather high mean amount can at least partly be reasoned by the survey design (talking about and showing pictures of the beauty of the forest and of future scenarios of damage) and the double-bounded DC questionnaire, and the occurrence of direct use values due to the high rate of visitors cannot be excluded. Also an interviewer effect cannot be denied, since the WTP in personal interviews usually is higher than in e-mail or mail surveys [36]. Furthermore, cultural conditions in this country may have influenced the stated WTP positively [37].
Veisten and Navrud [33] analyzed the WTP for the protection of old forests in Norway, a good nearly exclusively linked to passive-use values, using a mail survey among 2498 people in Norway conducted in 1995. The efficient total sample and overall response rate were 1792 and 71.7% respectively. According to the payment question format (open ended or dichotomous choice), estimated WTP values ranged from a mean of 20.5 US$ to 41.6 US$ in form of a one-time payment to the WWF’s Forest Fund. This corresponds to roughly 27€ to 61€ in 2020 with a rate of positive WTP of 29–46%. With an additional invoice for the stated WTP value, this value changed to 24–37% and a mean WTP value of 5$ to 11$, corresponding roughly to 7€ and 14€ in 2020. These values indicate that CV values are not only sensitive to the question format, but also to the scenario setting and the payment vehicle.
Broberg [34] used contingent valuation to estimate the public benefit derived from preserving 126,000 ha of state-owned old-growth forest in the sub-mountainous region of Sweden. In this mail survey, the response rate was 49%. About 45% of the 905 respondents had a positive WTP with an average of approximately SEK 300 (35€ in 2020) for the preservation program as an annual tax increase over the next 5 years. Males were significantly less likely to hold a positive WTP, and the likelihood decreased with age for both, males and females. Education, income, and membership in any environmental NGO were correlated positively with the likelihood of observing a positive WTP.
Table 1 provides an overview of the studies.
Although we searched broadly for comparable studies about environmental objectives with a symbolic character, besides few direct use values, we did not find any. Laplante et al. [38] surveyed the value of the Armenian lake Sevan for US American Residents with Armenian origin. They asked 6000 people about their willingness to participate in a mail survey, of which 1325 agreed to participate, but only 389 returned a completed questionnaire. The WTP was surveyed in form of DC as a one-time donation and led to a mean value between 80 US$ and 280 US$, which corresponds to 47€–118€ nowadays. Most significant variables for the WTP were past visits and the option of future visits of the lake. Thus, although the lake has a highly symbolic character, use values seemed to be most important for the WTP.
Even though the population of Germany is known for its love of wild forests [39, 40], there is currently no German study that explicitly addresses non-use values of forests. Compared with the studies above, the Hambach Forest is rather small given its size of only about 500 ha, and to almost all Germans, its value comprises passive-use values only. Therefore, even though it may be ecologically valuable, it is hardly comparable to the other evaluated woods and forests from an ecological point of view. Instead, it is especially its symbolic character that makes it a highly interesting research subject that justified its evaluation. Since no comparable situation analyzed by an evaluation survey so far was found, our study is of highly explorative character.
According to the literature review, CVM proposed itself to be the method of choice, since a high rate of existence value of the Hambach Forest was presumed for the German population. Ideally, the surveyed sample corresponds to the distribution of these variables across the basic population. In mail surveys, the sample selection bias is usually stronger than in telephone or personal inquiries [41, 42], making the latter more advisable as survey methods, although they are normally more expensive. We therefore decided to conduct the survey via telephone with strong instructions regarding the representativeness concerning age, gender, education, and place of residence (federal state). Furthermore, questions regarding attitudes toward environmental values and behavior, renewable and nonrenewable energy systems as well as political issues were included in our questionnaire.
Moreover, protest responses occur regularly in environmental valuation surveys [43]. They can be reduced by the survey design, however, since they are usually lower when voluntary payment schemes are provided [44]. As a procedure, it appeared useful in our case to contact participants personally following a random selection scheme in order to guarantee the representativeness due to the self-selection bias of online and mail surveys. Voluntary contributions to a fund seemed to be most adequate as a payment vehicle for several reasons: First, because of an expectedly high rate of passive-use values, payment vehicles linked to a certain kind of use dropped out. Second, due to a high level of politicization of the issue, a rather “neutral” instrument for the protection of the forest seemed to be preferable to a tax, for example. Third, the voluntary character of the payment scenario fit better to the climate protection movement, since the latter is strongly characterized by the perception that “policy isn’t doing enough to fight climate change” and that it is instead the people who need to take action now.
Therefore, the developed CV scenario was the following: “A bit over a year ago, the Hambach Forest was prevalently in the media, because it was uncertain whether vast parts of it should be cleared in favor of lignite mining and its electricity generation. Assume that a private forest conservation initiative would be founded, which relies on private donations to buy and maintain the forest, thereby preventing the lignite below it from being mined. Would you be willing to donate to such an initiative?”3 If respondents answered with “yes,” they were asked to indicate their hypothetical donation in Euros. Furthermore, based on the observed factors of relevance for the WTP from the literature survey, we also included questions about attitudes and habits regarding climate change, energy, and environmental issues, as well as the usual sociodemographic queries in our questionnaire.
The initial idea of our study was to conduct a cost-benefit analysis (CBA) under consideration of the use- and non-use values evaluated by the CV as well as of opportunity costs arising from the preservation of the forest for RWE and the region. The intention was to provide a rather neutral perspective on the highly politicized issue and support decision-makers in finding solutions by considering all aspects adequately. However, only four weeks after the survey was conducted in December 2019, the German government decided the early coal phase-out, also proposing that the preservation of the Hambach Forest should be guaranteed. Therefore, the focus of our analysis was broadened from the evaluation of the forest as such to the assessment of factors for a positive WTP for the Hambach Forest and the role of attitudes toward different forms of energy generation. Since the CV was part of a bigger survey about the German energy transition and the bioeconomy, questions regarding preferences for power generation technologies, methods from the field of bioeconomy as well as general attitudes regarding the environment were also included.
The survey was conducted by a professional agency in December 2019. Altogether, 1,002 people participated in the telephone survey. Data obtained from the national survey were analyzed using the statistical package IBM SPSS 19. The sample is almost representative of the German population in terms of age, gender, education, and city size and residence in the 12 German federal states. Regarding the number of people per household, single households were underrepresented in our sample (27.9% as compared with 41.9%), whereas households with two persons were overrepresented (40% as compared with 33.8%) [45]. The household income was approximately representative of the German population, with the restriction that 10% of the respondents refused to answer this question. Accordingly, the lowest and the highest income classes are underrepresented in our survey, which is in line with the common observation that people in extreme classes of income more often refuse to reveal their household income [46].
Altogether, 47.2% of the surveyed people stated to be willing to pay an amount between 3€ and 1000€ for the preservation of the Hambach Forest. Furthermore, 49.7% answered the question about their WTP with “no,” and 3.1% refused to provide an answer. In this case, a clear distinction between true zeros and protest zeros was not possible, since we did not ask for the reasons based on which they would refuse to pay. However, an indication for the occurrence of protest answer can be seen in the fact that 20% of the survey participants who stated a WTP of zero refused the further run of coal-fired power plants completely. For those with a positive WTP, the rate was 38%. According to a meta-analysis of Meyerhoff and Liebe [44], the mean share of protest responses in CV surveys is about 18% with a median value of 16%. The share is higher in scenarios with taxes or entrance fees as payment vehicle, and also the survey method may have an impact with onsite-, web-, and phone surveys leading to a lower share of protest zeros [44].
In order to observe differences between those with and those without a positive WTP for the preservation of the forest, we excluded all participants who did not answer this question with either “yes” or “no,” which resulted in a total of 971 cases. We observed no differences regarding the WTP per se in terms of sociodemographic aspects except that females were more likely to state a positive WTP than males (p = .05). Highly significant differences between the two groups were observed for revealed activities listed in question 5.2 (Table 2): “Which of the following did you do within the last 12 months?” People with a positive WTP were much more likely to confirm those. Correlation coefficients are calculated as Pearson’s r, since the variables were dichotomous (yes-no).
Measurement | Pearson’s r | Significance |
---|---|---|
(a) Selective buying of regional food | .185 | .000 |
(b) Selective buying of packages made of renewable materials | .247 | .000 |
(c) Purchase of green electricity | .164 | .000 |
(d) Avoidance of packaging | .185 | .000 |
(e) Adaptation of the mobility behavior (e.g., to abandon the car or to use the bicycle more often) | .234 | .000 |
(f) Purchase of bio-products | .271 | .000 |
(g) Carbon compensation (payment to a specific organization for carbon offsetting projects) | .079 | .014 |
Correlation between reported pro-environmental behavior (Q5.2) and a positive WTP.
Source: own.
Participants with a positive WTP also favored nearly all surveyed aspects of a renewable energies, including the application of biogas, biofuels, and renewables in the industry, more than those who were not willing to pay. Those who stated they were willing to pay rated themselves as more informed regarding the energy transition. Furthermore, they had a more positive attitude toward solar energy, wind turbines, water turbines, and energy from biomass. Accordingly, the same was observed with a negative correlation for coal-fired and nuclear power generation. Furthermore, they rated themselves as more informed regarding the coal phase-out. All of those correlations were significant at the 0.01%level. No significant differences between the two groups were found for attitudes toward conventional and nonconventional natural gasoline.
Those who refused to answer the question whether they would be willing to pay at all apparently have strong pro-environmental attitudes, even compared with those who stated a positive WTP. For example, all of the 31 respondents from this category answered Q5.2e whether they changed their mobility behavior, e.g., by taking more often the bicycle instead the car, with “yes,” while around 65% of those with a positive and 42% with a negative WTP affirmed this question. A similar distribution was observed for Q5.2d, whether respondents had consciously forgone packaging while doing groceries during the last 12 months. Those who refused and those who stated a positive WTP answered most other questions regarding attitudes and behavior toward environmental issues similarly.
For the analysis of the amount of the WTP, we omitted those 31 cases with no answer as to whether they would be willing to pay. Of the 971 considered cases, 498 (51.3%) declined a willingness to pay. For further analyses, we treated these values as true zeros, although it cannot be ruled out that, by doing so, protest zeros are neglected. Therefore, the results should be considered a conservative estimate, and real preferences might be higher. In a first step, we checked the theoretical validity of the stated amounts by analyzing some of the variables, such as the income and attitudinal variables [47]. The mean WTP for all participants, including the zero values, was 26.83€, and the most frequently stated positive value was 50€, provided by 124 participants (12.8%). The mean WTP considering only positive values was 55.08€, whereas about 10% of the sample had a WTP higher than 50€. The highest stated amount was 1000€, expressed by three survey participants. Since none of the three profiles provided an indication for unreliable values, due to high income, high education, and a strong attitude toward environmental issues, we did not exclude them from further analyses. The same correlations were also checked for the whole sample. As expected, significant positive correlations were observed between stated pro-environmental behavior of Q5.2 and the level of income. Furthermore, also significant positive correlations were observed for preferences for renewable energy technologies such as solar, wind, biomass, and hydro, and negative correlations for coal power and nuclear engineering. Here, again, no significant differences in attitudes regarding conventional and nonconventional natural gas were found. People who rated themselves as more informed regarding the coal phase-out also had a significantly higher WTP. When considering only cases with a positive WTP, no significant differences regarding preferences for energy technologies were observed. Regarding stated pro-environmental behavior, only minor significant correlations were observed for the acquisition of green energy Q5.2c (positively) and the adaptation of the mobility behavior Q5.2e (negatively). Furthermore, people living in an owned house or flat, bigger household size, and higher income were linked to a significantly higher WTP. Although females had a significantly higher WTP overall, males with a positive WTP stated significantly higher amounts.
Even though the Hambach Forest seems to no longer be immediately threatened in the near future, an extrapolation of the stated WTP values is of high interest, for example, in order to be able to compare the stated value to those of other natural goods. As discussed, the estimation is rather conservative, since we did not exclude potential protest zeros, which generally account for between 5% and 50% [43, 48]. Given the representative character of the survey for the German population, an extrapolation of the mean value of 26.83€ for the full-age population of Germany, which is about 67 million people [49], would result in roughly 1.8 billion € without considering benefits for future generations and people outside of Germany. This correlates to roughly 3.6 million € per ha. However, the following points may have led to a higher estimated value:
Protest zeros are not considered.
Non-respondents hold above-average pro-environmental values in this case, which could be an indication for a high estimation for the preservation of the Hambach Forest, although they apparently would not or could not monetarize their preferences.
People with preferences for the scenario outside of Germany are not considered.
On the other hand, we did not provide the opportunity to state a quasi-negative WTP for our scenario to account for the fact that people might also be willing to pay in order to avoid the preservation of the Hambach Forest and favor instead the continuation of the original lignite mining plan. Just to compare these values, in North Rhine-Westphalia, the prices for forest areas—mainly working forest—in 2020 range from 10,000 to 30,000€ per ha according to a sales platform.
In order to generate an understanding of the importance of different factors influencing the willingness or non-willingness to pay, we conducted a binary logistic regression. Our hypotheses were that people with more pro-environmental behavior, pro-environmental attitudes, preferences for fossil-free power generation, and younger people are more willing to pay. Accordingly, attitudes toward the environment and energy technologies appeared to be important as impact factors, as well as gender and age. We also tested both, schooling and vocational education, but neither had significant impact on the dependent variable within the binary logistic regression model and were thus left out (Table 3). Our final model consists of six variables and considers 971 cases, representing roughly 97% of the sample. The remaining cases were excluded due to missing values regarding the dependent variable. A check for multicollinearity of the explaining variables showed no critical values. Using our binary logistic regression model, the rate of correctly predicted values rose from 51.3% to 66.9%. The pseudo-R squared (Nagelkerke) is 0.207, which is “acceptable” according to Backhaus et al. [50].
B | S.E. | Wald | df | Sig. | Exp(B) | |
---|---|---|---|---|---|---|
Attitudes toward renewables Q2.1 a-d | .300 | .112 | 7.189 | 1 | .007 | 1.350 |
Age (years) Q8.1.2 | −.009 | .004 | 4.078 | 1 | .043 | .991 |
Gender (male) Q8.1.1 | −.245 | .144 | 2.899 | 1 | .089 | .783 |
Pro-environmental behavior Q5.2 | .371 | .045 | 68.672 | 1 | .000 | 1.449 |
Eco-centered conviction Q7.8.3 | .128 | .051 | 6.375 | 1 | .012 | 1.136 |
Attitude toward lignite Q2.1e | −.156 | .043 | 12.953 | 1 | .000 | .856 |
Constant | −1.397 | .398 | 12.350 | 1 | .000 | .247 |
Parameter estimate of the binary logistic regression.
B: coefficient for the standard; S.E.: standard error for the coefficient around the constant; Wald: Wald Chi Square statistics; df: degree of freedom for the Wald Chi Square test; Exp (B): exponentiation of B coefficient, which is an odds ratio. Source: own.
Table 3 illustrates the influence of nearly each predictor variable, except gender, to the logistic model and the statistical significance (p < .05) of the Wald Chi Square test, which is obtained by squaring the ratio of the regression coefficient (B) to its standard error (S.E.). According to our analysis, the stated pro-environmental behavior, which normally correlates with strong pro-environmental attitudes, has the strongest impact on the WTP. This observation is not surprising, and this strong relationship has been shown by various studies (e.g., [51, 52]). The Odds Ratio (Exp(B)) indicates that, if the stated pro-environmental behavior increases by one unit, the probability to state a positive WTP increases by roughly 45%. The second largest impact factor is the attitude toward renewable energies (solar, wind, hydro, and biomass), which is also correlated significantly with stated pro-environmental behavior; an increase of one unit here implicates an increase of probability by 35%. This observation supports the assumption that not only values of the forest, but also a favor for the energy transition may have played a role in the decision to state a positive WTP. Further, an eco-centered conviction, measured by a statement regarding the perception of the vulnerability of the earth (Q7.8.3), has a clear positive impact on the WTP, although it is comparatively small. The acceptance of the use of lignite as an energy source (Q2.1e), instead, has a negative impact on the WTP; an increase by one unit of acceptance implies a decrease of roughly 14% in the probability to state a positive WTP. A negative impact on the probability to state a positive WTP can be observed for age and being male, although on a rather low level of significance. According to the literature, no general impact of gender on the WTP for environmental goods can be observed, since other factors such as attitudes, education, or income are generally more important [53]. However, a recent survey found that females probably are more pro-environmental in both Germany and the Netherlands [54]. By separating age from other factors, sometimes a negative impact can be observed, which means that older people are less willing to pay for environmental issues [53]. In these regards, our results are thus in line with previous findings.
In order to detect significant impact factors on the stated monetary values for the protection of the Hambach Forest, we conducted an OLS regression analysis. The dependent variable, the stated amount of those willing to pay, was rather log-normal than normally distributed. Therefore, we logarithmized the dependent variable and applied a semi-log model. The following explanatory variables were considered:
stated behavior regarding the environment (Q5.2),
household income (Q8.6),
age (Q8.1.2),
gender (Q8.1.1),
stated preferences for the renewables (Q2.1),
attitudes toward lignite (Q2.1e),
trust in the national and federal government (Q6.1a and Q6.1b),
political party, which was chosen during the national election in 2017 (Q7.3),
satisfaction with the way political decisions are conducted in Germany (Q7.4),
perception of the vulnerability of the earth (Q7.8c).
However, only a very low rate of explained variation with an R2 of .081 and a corrected R2 of .057 could be reached using an OLS regression approach. The results are displayed in Table 4. No more than three variables with significant impact on the stated amount of the WTP were observed: gender (p = .01), household income (p = .001), and the degree of agreement with statement Q7.8c about the vulnerability of the earth (p = .05). As generally the case in CVs, household income has a positive effect on the WTP: the higher the income, the more easily people can afford to pay for environmental goods and services. Compared with the other variables, income had the strongest impact on the WTP, but only when considering the average household income. In other models, when per-capita income was considered the explaining variable, no significant impact was observable. Furthermore, in our case also being male had a positive impact on the WTP. It is important to note that males had a significantly higher household income in our survey. However, testing for collinearity did not reveal problematic values. Finally, the impact of perceived higher vulnerability of the earth on the WTP can be considered as an indicator for a higher estimation of existence values as well as fears of losses of environmental goods and services. Stronger agreement with this statement normally goes along with a more nature-centered point of view, which also could explain a higher WTP. The low rate of explained variation leads to the assumption that other factors, which we did not consider in our survey, may be of strong relevance for the stated amount. Imaginable are issues regarding personal budget constraints, a general estimation of woods and forests, or dissatisfaction with climate policies, as well as embedding effects resulting from our payment scenario. Alternatively, the group of respondents with a positive WTP is more homogeneous regarding attitudinal values compared with the same values over all respondents, as an analysis of variance showed.
Modell | Non-standardized coefficients | Standardized coefficients | T | Sig. | |
---|---|---|---|---|---|
Regression coefficient B | Standard error | Beta | |||
Constant | 2.401 | .434 | 5.531 | .000 | |
Attitude toward lignite Q2.1e | .031 | .030 | .051 | 1.021 | .308 |
Trust in the national government Q6.1a | −.027 | .047 | −.049 | −.570 | .569 |
Trust in the federal government Q6.1b | .069 | .049 | .120 | 1.415 | .158 |
Perception of the vulnerability of the earth Q7.8c | .088 | .035 | .124 | 2.512 | .012 |
Age (years) Q8.1.2 | .003 | .003 | .054 | 1.085 | .279 |
Summary of pro-environmental behavior Q5.2 | .001 | .032 | .002 | .045 | .964 |
Summary of attitudes toward solar power, wind power, water power, and energy from biomass Q2.1 | −.001 | .056 | −.001 | −.010 | .992 |
Voted the Green party at the last national election Q7.3 | .087 | .119 | .036 | .726 | .468 |
Gender: Male Q8.1.1 | .272 | .097 | .137 | 2.793 | .005 |
Household income Q8.6 | .000 | .000 | .184 | 3.799 | .000 |
Attitude toward the end of lignite mining Q4.3 | −.143 | .097 | −.077 | -1.470 | .142 |
Parameter estimate of the OLS regression.
Dependent Variable: LogNormal_0_WTP.
Source: own.
Striking outcome of our survey results is that, against our expectations, no clear differences in the results were found compared with earlier surveys about stated WTP values of forests. All of the results are more or less in line with previous findings about values for environmental goods [20, 55]. This is especially interesting, since in this case nearly exclusively existence values are of relevance, whereas the other cited surveys mostly consider also direct use values. Kriström [56] found that respondents who expressed only a use motive stated a higher WTP on average than respondents stating only a non-use motive. Those who expressed both, use and non-use motives, stated the highest WTP. Since the stated values here are quite similar to those of the other cases described in the literature review section, this may be seen as an indicator for the existence of a premium for a symbolic value on top of already known non-use values. The variable with the highest impact on the WTP was income, which can be interpreted as an indicator for reliability of the stated amounts [57]. However, in contrast to most other surveys about environmental goods, this time only passive-use values were of relevance. Further, the area of the Hambach Forest is rather small compared with other woods and forests evaluated so far. Thus, WTP values referring to the area lead to an exceptionally high value compared with previous surveys [20] based on passive-use values only. There is a long-lasting discussion about the sensitivity of scope in contingent valuation surveys [55, 58, 59, 60, 61, 62, 63, 64, 65]. Inconsistencies are quite often a result of a lack of spatial sense: only a minority has a clear image of, e.g., 10,000 ha or 50,000 cormorants. However, in cases where existence values dominate over use values, scope is usually of minor relevance for the stated WTP [61, 63]. Lindhjem [35] found in a meta-analysis of Scandinavian WTP surveys for woods and forests only minor scope effects, whereas he argues that woods and forests are complex environmental goods, and simplified indicators such as area size or percentage may not easily capture their scope. Hjerpe et al. [63], in contrast, found that individuals are typically sensitive to the scope of ecosystem service provision, in both quality and quantity. Also Ojea and Loureiro [65] found that CV results are sensitive to the scope of the good being valued, but the results depend on how the environmental change is measured: absolute sizes are preferable over relative ones. Further, Barrio and Loureiro [55] found out that, among others, recreational aspects play an important role for the WTP of people for the preservation of forests. It is therefore possible that the following two effects might have led to “normal” WTP values in our case: the nearly total absence of direct use values might have lowered the WTP for the Hambach Forest, whereas the threat of a drastic change in form of a complete annihilation might have had an opposite effect. Further, the already mentioned symbolic value is reflected in the stated WTP values.
Regarding the results from the regression analyses, the remarkable difference in the rate of explained variance is astonishing: while the decision to be willing to pay or not could reach an acceptable level of explained variance by a regression model, the explained variance for the stated amount remained on a low level. This means that some underlying factors seem to exist, which are not covered by the survey. Imaginable are attitudes toward the procedure of the policy administration in this case, which initiated a strong and disproportionate police operation, in which the Hambach Forest should be freed from occupants and thus also be prepared for a quick clearance, in case of need. Another possible explanation may be a considerable rate of protest responses in our survey. Furthermore, in the view of parts of the population, RWE is often portrayed as voracious based on the fact that it is responsible for having already effaced the largest part of the Hambach Forest and for planning to annihilate it completely. Therefore, the will to contribute to a fund, which prevents the complete annihilation of the forest, may also result from a desire to stop RWE in following its operating plan. The concern of climate change and its mitigation may have played an additional role, since 2018 and 2019 were the first and the third hottest year in Germany since the beginning of the weather recordkeeping. Furthermore, this development was accompanied by the Fridays for Future movement initiated by Greta Thunberg and may thus also have contributed to the wish to combat climate change. Altogether, an interplay of different influencing factors on an individual basis seems to have led to the rather low level of explained variance of the stated WTP values.
We conducted a representative CV survey within the German population in order to find out whether there is a symbolic value of the Hambach Forest. It is a remarkable statement for the preservation of the Hambach Forest that at least 47% of the respondents stated a positive WTP, considering that the forest does not provide any direct use values to almost all of the surveyed people. The mean value of the positive WTP was rather high with 55.08€, whereas the standard deviation of the stated values with about 76€ indicates considerable differences regarding attitude and estimation toward the Hambach Forest. Due to the almost complete absence of use values, the stated WTP can be seen as a premium for the existence of the Hambach Forest and as a vote against political decisions regarding lignite mining operation, climate protection, and the acceptance of coal fired power plants, as our regression analyses showed. Further, since the Hambach Forest provides nearly exclusively passive use values, and the WTP values are at least at the same level as in previous surveys with larger forests comprising also direct use values, this can be considered an indication for a premium for its symbolic value. Not least the strong media coverage with very different views reflects the broad spectrum of attitudes toward the Hambach Forest. People who are trying to act more environmentally benign also were significantly more likely to be willing to pay for the preservation of the Hambach Forest. Furthermore, their attitudes toward renewable energies were significantly more positive compared with those without a positive WTP. The symbolic status of the Hambach Forest can be characterized by opposites. For those who rather support the protests, the contrasts might be nature—destruction, climate protection—climate catastrophe, small (population)—big (RWE and provincial government), commons/common welfare—greed/profit. For those who are rather critical toward the protests, the case may represent the defense of jobs, welfare, law, and order against chaos, cadgers, and violent anarchists. Thus, a stated positive WTP can be an indicator for the self-identification of the respondents, whereas due to the unknown rate of protest zeros, the opposite is not so easy to state. A more in-depth analysis would be needed in order to answer the question about the motives of the respondents more profoundly.
Through our survey, we were able to show that the Hambach Forest holds a high valuation among the German population, which is nearly exclusively based on non-use values only, in which a premium for its symbolic value might be included. Considering the results of the CV question and bearing in mind that there is probably a non-negligible proportion of protest zeros, the valuation of the forest as a symbol against climate change is remarkable and should be considered in future political decisions. Especially for the background of the European Green Deal, which means that the European Union aims to become the world’s first “climate-neutral bloc” by 2050, these values might be understood as a hint for people’s support of an ambitious environmental and climate policy.
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He is the president of the Travel Medicine Committee of the Pan-American Infectious Diseases Association (API), as well as the president of the Colombian Association of Infectious Diseases (ACIN). He is a member of the Committee on Tropical Medicine, Zoonoses, and Travel Medicine of ACIN. He is a vice-president of the Latin American Society for Travel Medicine (SLAMVI) and a Member of the Council of the International Society for Infectious Diseases (ISID). Since 2014, he has been recognized as a Senior Researcher, at the Ministry of Science of Colombia. He is a professor at the Faculty of Medicine of the Fundacion Universitaria Autonoma de las Americas, in Pereira, Risaralda, Colombia. 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. His Scopus H index is 47 (Google Scholar H index, 68).",institutionString:"Institución Universitaria Visión de las Américas, Colombia",institution:null},{id:"332819",title:"Dr.",name:"Chukwudi Michael",middleName:"Michael",surname:"Egbuche",slug:"chukwudi-michael-egbuche",fullName:"Chukwudi Michael Egbuche",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/332819/images/14624_n.jpg",biography:"I an Dr. Chukwudi Michael Egbuche. I am a Senior Lecturer in the Department of Parasitology and Entomology, Nnamdi Azikiwe University, Awka.",institutionString:null,institution:{name:"Nnamdi Azikiwe University",country:{name:"Nigeria"}}},{id:"284232",title:"Mr.",name:"Nikunj",middleName:"U",surname:"Tandel",slug:"nikunj-tandel",fullName:"Nikunj Tandel",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/284232/images/8275_n.jpg",biography:'Mr. Nikunj Tandel has completed his Master\'s degree in Biotechnology from VIT University, India in the year of 2012. He is having 8 years of research experience especially in the field of malaria epidemiology, immunology, and nanoparticle-based drug delivery system against the infectious diseases, autoimmune disorders and cancer. He has worked for the NIH funded-International Center of Excellence in Malaria Research project "Center for the study of complex malaria in India (CSCMi)" in collaboration with New York University. The preliminary objectives of the study are to understand and develop the evidence-based tools and interventions for the control and prevention of malaria in different sites of the INDIA. Alongside, with the help of next-generation genomics study, the team has studied the antimalarial drug resistance in India. Further, he has extended his research in the development of Humanized mice for the study of liver-stage malaria and identification of molecular marker(s) for the Artemisinin resistance. At present, his research focuses on understanding the role of B cells in the activation of CD8+ T cells in malaria. 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She is currently an Adjunct Professor at Feevale University in Medicine and Biomedicine courses and a permanent professor of the Academic Master\\'s Degree in Virology. She has experience in the field of Microbiology, with an emphasis on Bacteriology, working mainly on the following topics: bacteriophages, bacterial resistance, clinical microbiology and food microbiology.",institutionString:null,institution:{name:"Universidade Feevale",country:{name:"Brazil"}}},{id:"229220",title:"Dr.",name:"Amjad",middleName:"Islam",surname:"Aqib",slug:"amjad-aqib",fullName:"Amjad Aqib",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/229220/images/system/229220.png",biography:"Dr. Amjad Islam Aqib obtained a DVM and MSc (Hons) from University of Agriculture Faisalabad (UAF), Pakistan, and a PhD from the University of Veterinary and Animal Sciences Lahore, Pakistan. Dr. Aqib joined the Department of Clinical Medicine and Surgery at UAF for one year as an assistant professor where he developed a research laboratory designated for pathogenic bacteria. Since 2018, he has been Assistant Professor/Officer in-charge, Department of Medicine, Manager Research Operations and Development-ORIC, and President One Health Club at Cholistan University of Veterinary and Animal Sciences, Bahawalpur, Pakistan. He has nearly 100 publications to his credit. His research interests include epidemiological patterns and molecular analysis of antimicrobial resistance and modulation and vaccine development against animal pathogens of public health concern.",institutionString:"Cholistan University of Veterinary and Animal Sciences",institution:null},{id:"62900",title:"Prof.",name:"Fethi",middleName:null,surname:"Derbel",slug:"fethi-derbel",fullName:"Fethi Derbel",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/62900/images/system/62900.jpeg",biography:"Professor Fethi Derbel was born in 1960 in Tunisia. He received his medical degree from the Sousse Faculty of Medicine at Sousse, University of Sousse, Tunisia. He completed his surgical residency in General Surgery at the University Hospital Farhat Hached of Sousse and was a member of the Unit of Liver Transplantation in the University of Rennes, France. He then worked in the Department of Surgery at the Sahloul University Hospital in Sousse. Professor Derbel is presently working at the Clinique les Oliviers, Sousse, Tunisia. His hospital activities are mostly concerned with laparoscopic, colorectal, pancreatic, hepatobiliary, and gastric surgery. He is also very interested in hernia surgery and performs ventral hernia repairs and inguinal hernia repairs. He has been a member of the GREPA and Tunisian Hernia Society (THS). During his residency, he managed patients suffering from diabetic foot, and he was very interested in this pathology. For this reason, he decided to coordinate a book project dealing with the diabetic foot. Professor Derbel has published many articles in journals and collaborates intensively with IntechOpen Access Publisher as an editor.",institutionString:"Clinique les Oliviers",institution:null},{id:"300144",title:"Dr.",name:"Meriem",middleName:null,surname:"Braiki",slug:"meriem-braiki",fullName:"Meriem Braiki",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/300144/images/system/300144.jpg",biography:"Dr. Meriem Braiki is a specialist in pediatric surgeon from Tunisia. She was born in 1985. She received her medical degree from the University of Medicine at Sousse, Tunisia. She achieved her surgical residency training periods in Pediatric Surgery departments at University Hospitals in Monastir, Tunis and France.\r\nShe is currently working at the Pediatric surgery department, Sidi Bouzid Hospital, Tunisia. Her hospital activities are mostly concerned with laparoscopic, parietal, urological and digestive surgery. She has published several articles in diffrent journals.",institutionString:"Sidi Bouzid Regional Hospital",institution:null},{id:"229481",title:"Dr.",name:"Erika M.",middleName:"Martins",surname:"de Carvalho",slug:"erika-m.-de-carvalho",fullName:"Erika M. de Carvalho",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/229481/images/6397_n.jpg",biography:null,institutionString:null,institution:{name:"Oswaldo Cruz Foundation",country:{name:"Brazil"}}},{id:"186537",title:"Prof.",name:"Tonay",middleName:null,surname:"Inceboz",slug:"tonay-inceboz",fullName:"Tonay Inceboz",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/186537/images/system/186537.jfif",biography:"I was graduated from Ege University of Medical Faculty (Turkey) in 1988 and completed his Med. PhD degree in Medical Parasitology at the same university. I became an Associate Professor in 2008 and Professor in 2014. I am currently working as a Professor at the Department of Medical Parasitology at Dokuz Eylul University, Izmir, Turkey.\n\nI have given many lectures, presentations in different academic meetings. I have more than 60 articles in peer-reviewed journals, 18 book chapters, 1 book editorship.\n\nMy research interests are Echinococcus granulosus, Echinococcus multilocularis (diagnosis, life cycle, in vitro and in vivo cultivation), and Trichomonas vaginalis (diagnosis, PCR, and in vitro cultivation).",institutionString:"Dokuz Eylül University",institution:{name:"Dokuz Eylül University",country:{name:"Turkey"}}},{id:"71812",title:"Prof.",name:"Hanem Fathy",middleName:"Fathy",surname:"Khater",slug:"hanem-fathy-khater",fullName:"Hanem Fathy Khater",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/71812/images/1167_n.jpg",biography:"Prof. Khater is a Professor of Parasitology at Benha University, Egypt. She studied for her doctoral degree, at the Department of Entomology, College of Agriculture, Food and Natural Resources, University of Missouri, Columbia, USA. She has completed her Ph.D. degrees in Parasitology in Egypt, from where she got the award for “the best scientific Ph.D. dissertation”. She worked at the School of Biological Sciences, Bristol, England, the UK in controlling insects of medical and veterinary importance as a grant from Newton Mosharafa, the British Council. Her research is focused on searching of pesticides against mosquitoes, house flies, lice, green bottle fly, camel nasal botfly, soft and hard ticks, mites, and the diamondback moth as well as control of several parasites using safe and natural materials to avoid drug resistances and environmental contamination.",institutionString:null,institution:{name:"Banha University",country:{name:"Egypt"}}},{id:"99780",title:"Prof.",name:"Omolade",middleName:"Olayinka",surname:"Okwa",slug:"omolade-okwa",fullName:"Omolade Okwa",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/99780/images/system/99780.jpg",biography:"Omolade Olayinka Okwa is presently a Professor of Parasitology at Lagos State University, Nigeria. She has a PhD in Parasitology (1997), an MSc in Cellular Parasitology (1992), and a BSc (Hons) Zoology (1990) all from the University of Ibadan, Nigeria. She teaches parasitology at the undergraduate and postgraduate levels. She was a recipient of a Commonwealth fellowship supported by British Council tenable at the Centre for Entomology and Parasitology (CAEP), Keele University, United Kingdom between 2004 and 2005. She was awarded an Honorary Visiting Research Fellow at the same university from 2005 to 2007. \nShe has been an external examiner to the Department of Veterinary Microbiology and Parasitology, University of Ibadan, MSc programme between 2010 and 2012. She is a member of the Nigerian Society of Experimental Biology (NISEB), Parasitology and Public Health Society of Nigeria (PPSN), Science Association of Nigeria (SAN), Zoological Society of Nigeria (ZSN), and is Vice Chairperson of the Organisation of Women in Science (OWSG), LASU chapter. She served as Head of Department of Zoology and Environmental Biology, Lagos State University from 2007 to 2010 and 2014 to 2016. She is a reviewer for several local and international journals such as Unilag Journal of Science, Libyan Journal of Medicine, Journal of Medicine and Medical Sciences, and Annual Research and Review in Science. \nShe has authored 45 scientific research publications in local and international journals, 8 scientific reviews, 4 books, and 3 book chapters, which includes the books “Malaria Parasites” and “Malaria” which are IntechOpen access publications.",institutionString:"Lagos State University",institution:{name:"Lagos State University",country:{name:"Nigeria"}}},{id:"273100",title:"Dr.",name:"Vijay",middleName:null,surname:"Gayam",slug:"vijay-gayam",fullName:"Vijay Gayam",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/273100/images/system/273100.jpeg",biography:"Dr. Vijay Bhaskar Reddy Gayam is currently practicing as an internist at Interfaith Medical Center in Brooklyn, New York, USA. He is also a Clinical Assistant Professor at the SUNY Downstate University Hospital and Adjunct Professor of Medicine at the American University of Antigua. He is a holder of an M.B.B.S. degree bestowed to him by Osmania Medical College and received his M.D. at Interfaith Medical Center. His career goals thus far have heavily focused on direct patient care, medical education, and clinical research. He currently serves in two leadership capacities; Assistant Program Director of Medicine at Interfaith Medical Center and as a Councilor for the American\r\nFederation for Medical Research. As a true academician and researcher, he has more than 50 papers indexed in international peer-reviewed journals. He has also presented numerous papers in multiple national and international scientific conferences. His areas of research interest include general internal medicine, gastroenterology and hepatology. He serves as an editor, editorial board member and reviewer for multiple international journals. His research on Hepatitis C has been very successful and has led to multiple research awards, including the 'Equity in Prevention and Treatment Award” from the New York Department of Health Viral Hepatitis Symposium (2018) and the 'Presidential Poster Award” awarded to him by the American College of Gastroenterology (2018). He was also awarded 'Outstanding Clinician in General Medicine” by Venus International Foundation for his extensive research expertise and services, perform over and above the standard expected in the advancement of healthcare, patient safety and quality of care.",institutionString:"Interfaith Medical Center",institution:{name:"Interfaith Medical Center",country:{name:"United States of America"}}},{id:"93517",title:"Dr.",name:"Clement",middleName:"Adebajo",surname:"Meseko",slug:"clement-meseko",fullName:"Clement Meseko",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/93517/images/system/93517.jpg",biography:"Dr. Clement Meseko obtained DVM and PhD degree in Veterinary Medicine and Virology respectively. He has worked for over 20 years in both private and public sectors including the academia, contributing to knowledge and control of infectious disease. Through the application of epidemiological skill, classical and molecular virological skills, he investigates viruses of economic and public health importance for the mitigation of the negative impact on people, animal and the environment in the context of Onehealth. \r\nDr. Meseko’s field experience on animal and zoonotic diseases and pathogen dynamics at the human-animal interface over the years shaped his carrier in research and scientific inquiries. He has been part of the investigation of Highly Pathogenic Avian Influenza incursions in sub Saharan Africa and monitors swine Influenza (Pandemic influenza Virus) agro-ecology and potential for interspecies transmission. He has authored and reviewed a number of journal articles and book chapters.",institutionString:"National Veterinary Research Institute",institution:{name:"National Veterinary Research Institute",country:{name:"Nigeria"}}},{id:"158026",title:"Prof.",name:"Shailendra K.",middleName:null,surname:"Saxena",slug:"shailendra-k.-saxena",fullName:"Shailendra K. Saxena",position:null,profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRET3QAO/Profile_Picture_2022-05-10T10:10:26.jpeg",biography:"Professor Dr. Shailendra K. Saxena is a vice dean and professor at King George's Medical University, Lucknow, India. His research interests involve understanding the molecular mechanisms of host defense during human viral infections and developing new predictive, preventive, and therapeutic strategies for them using Japanese encephalitis virus (JEV), HIV, and emerging viruses as a model via stem cell and cell culture technologies. His research work has been published in various high-impact factor journals (Science, PNAS, Nature Medicine) with a high number of citations. He has received many awards and honors in India and abroad including various Young Scientist Awards, BBSRC India Partnering Award, and Dr. JC Bose National Award of Department of Biotechnology, Min. of Science and Technology, Govt. of India. Dr. Saxena is a fellow of various international societies/academies including the Royal College of Pathologists, United Kingdom; Royal Society of Medicine, London; Royal Society of Biology, United Kingdom; Royal Society of Chemistry, London; and Academy of Translational Medicine Professionals, Austria. He was named a Global Leader in Science by The Scientist. He is also an international opinion leader/expert in vaccination for Japanese encephalitis by IPIC (UK).",institutionString:"King George's Medical University",institution:{name:"King George's Medical University",country:{name:"India"}}},{id:"94928",title:"Dr.",name:"Takuo",middleName:null,surname:"Mizukami",slug:"takuo-mizukami",fullName:"Takuo Mizukami",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/94928/images/6402_n.jpg",biography:null,institutionString:null,institution:{name:"National Institute of Infectious Diseases",country:{name:"Japan"}}},{id:"233433",title:"Dr.",name:"Yulia",middleName:null,surname:"Desheva",slug:"yulia-desheva",fullName:"Yulia Desheva",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/233433/images/system/233433.png",biography:"Dr. Yulia Desheva is a leading researcher at the Institute of Experimental Medicine, St. Petersburg, Russia. She is a professor in the Stomatology Faculty, St. Petersburg State University. She has expertise in the development and evaluation of a wide range of live mucosal vaccines against influenza and bacterial complications. 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