Dissertations / Theses on the topic 'Prey'
Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles
Consult the top 50 dissertations / theses for your research on the topic 'Prey.'
Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.
You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.
Browse dissertations / theses on a wide variety of disciplines and organise your bibliography correctly.
Sun, Jing. "Prey." Thesis, California State University, Los Angeles, 2018. http://pqdtopen.proquest.com/#viewpdf?dispub=10787932.
Full textThe primary purpose of my research is to visually represent what can be regarded as a traditional Chinese thinking system and artistic style. This is to gain a deeper understanding of typical problem-solving processes of the Chinese culture. Through this research, I intend to encourage a bridge of communication between American and other cultures. It is my intent to help analyze problem-solving traditions in Chinese culture, and present a narrative that dramatizes this. The goal of this thesis; therefore, is to give a path of connection and appreciation for those not familiar, to a deeper understanding of contextualized Chinese beliefs. My process is aimed at constructing an effective narrative that illustrates the way a society creates change, in order to reflect broader cultural exchange and communication. The inspiration to undertake this study came from my three years’ of living in Los Angeles. Being suddenly transplanted into American culture made me critically review my own cultural beliefs. I often experienced cases of “misunderstandings” or “conflicts”. I perceived issues that were often embedded in the different ways that various cultures viewed and dealt with similar problems. There were, of course, differences in problem solving strategies, alongside differences in aesthetics, and perception. Consequently, based on these observations, I began to analyze how contrasting viewpoints and strategies could be translated into an animated narrative, and I wondered how I could effectively achieve this. Through this process, I addressed problems or crisis within various types of political systems. Can the methodology one uses to solve a problem be seen as systematic of the process of their own culture, even though the end goals and difficulties faced may be similar throughout various cultures? To critically analyze this question, I combined narrative animation and graphic watercolor renderings that visually parallel my personal experience of what could be defined as exemplary of traditional Chinese thought. An animated film resulted from this process, along with further research aimed at stimulating the public to appreciate the underlying approaches in both traditional Chinese aesthetics and culture. With this research, I intend to stimulate positive connections and appreciation between all cultures—a sentiment that extends to having increased inter-cultural communication and exchanges.
Martin, Annik. "Predator-prey models with delays and prey harvesting." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1999. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape9/PQDD_0016/MQ49407.pdf.
Full textQuinones, Paige Valentine. "The Best Prey." The Ohio State University, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=osu1461176139.
Full textKirkland, Shauna. "Birds of Prey." VCU Scholars Compass, 2013. http://scholarscompass.vcu.edu/etd/3019.
Full textMiner, Jeffrey G. "Turbidity-mediated predator-prey interactions among piscivores, prey fishes, and zooplankton /." The Ohio State University, 1990. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487685204970099.
Full textRosner, Tammy Dee. "Spatial predator-prey dynamics, the effect of prey movement and environmental heterogeneity." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1999. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp01/MQ38608.pdf.
Full textKato, Motomi. "Effects of enrichment on one-predator-two-prey systems with different prey profitability." 京都大学 (Kyoto University), 2001. http://hdl.handle.net/2433/86465.
Full textLindström, Torsten. "Predator-prey systems and applications." Licentiate thesis, Luleå tekniska universitet, 1991. http://urn.kb.se/resolve?urn=urn:nbn:se:ltu:diva-25928.
Full textLiu, Shouzong. "AGE-STRUCTURED PREDATOR-PREY MODELS." OpenSIUC, 2018. https://opensiuc.lib.siu.edu/dissertations/1577.
Full textReif, V. (Vitali). "Birds of prey and grouse in Finland:do avian predators limit or regulate their prey numbers?" Doctoral thesis, University of Oulu, 2008. http://urn.fi/urn:isbn:9789514288050.
Full textClements, Hayley Susan. "Incorporating prey demographics and predator social structure into prey selection and carrying capacity estimates for cheetah." Thesis, Nelson Mandela Metropolitan University, 2012. http://hdl.handle.net/10948/d1018606.
Full textGourley, Stephen Alexander. "Nonlocal effects in predator prey systems." Thesis, University of Bath, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.332378.
Full textMay, Celia A. "VNTR studies of birds of prey." Thesis, University of Nottingham, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.358003.
Full textBrighton, Caroline. "Attack strategies in birds of prey." Thesis, University of Oxford, 2016. https://ora.ox.ac.uk/objects/uuid:4e8afdec-3b7b-43b1-a693-166d114c827f.
Full textChrobok, Viktor. "Harvesting in the Predator - Prey Model." Master's thesis, Vysoká škola ekonomická v Praze, 2009. http://www.nusl.cz/ntk/nusl-10510.
Full textJohannesen, Asa. "Predator-prey interactions in aquatic environments." Thesis, University of Leeds, 2013. http://etheses.whiterose.ac.uk/7556/.
Full textShek, Lok Lun. "Oxygen consumption rate of copepod fecal pellets : variations among copepod species, prey types and prey nutritional values /." View abstract or full-text, 2010. http://library.ust.hk/cgi/db/thesis.pl?ENVR%202010%20SHEK.
Full textBecker, Matthew Smith. "Applying predator-prey theory to evaluate large mammal dynamics wolf predation in a newly-established multiple-prey system /." Thesis, Montana State University, 2008. http://etd.lib.montana.edu/etd/2008/becker/BeckerM1208.pdf.
Full textCresswell, Will. "Wintering raptors and their avian prey : a study of the behavioural and ecological effects of predator-prey interactions." Thesis, University of Edinburgh, 1993. http://hdl.handle.net/1842/14744.
Full textCantryll-Stewart, Ricki. "A discernment of prey selection by the ancient Maya : white-tailed deer (Odocoileus virginianus) : pest, prey, or domesticate." Thesis, University of Nottingham, 2018. http://eprints.nottingham.ac.uk/50198/.
Full textJohansson, Markus, and Martin Torstensson. "Hostile Takeovers : The Power of the Prey." Thesis, Jönköping University, JIBS, Business Administration, 2008. http://urn.kb.se/resolve?urn=urn:nbn:se:hj:diva-1321.
Full textTakeovers are used as a mean for companies to grow and gain entry to new markets. Hos-tile takeovers, apart from the friendly takeovers, is when an acquirer tries to takeover a corporation against the will of management, shareholders and board of directors of the target company. All listed companies run the risk of being a target for a hostile takeover, and to-day many companies are trying to involve actions protecting them from possible threats. Lacking protection can evolve into a costly defense program with actions with fictitious names such as White knight, Pac-man and Poison pills. The purpose with this thesis is to describe and analyze hostile takeovers and hostile takeover attempts in Sweden, and the defense tactics involved in the process.
In this thesis a deductive approach will be used, where theories are used as guidance when searching for explanations. On the basis of the defense tactics described in the theory empirical data has been gathered with the purpose of seeing if the expectations reflect reality, and conclusions about their efficiency. The thesis has used a quantitative research method where the focus is on what, where and when. The aim of the thesis is to classify targeted features and count them, with the intent to construct statistical models with an underlying purpose of explaining what is observed.
The most frequently used defense tactic used by the target company in a hostile takeover in the Swedish market is to attack the logic of the bid. Around 56 percent of the targets in a hostile takeover or a hostile takeover attempt have used this defense tactic to avoid a hos-tile takeover. The aim with an implemented defense tactic is to avoid a hostile bid or making it impossible for the hostile bidder to proceed with the bid and close the deal. The White knight and White squire defense tactic is the most successful defense tactic when it comes to not finalizing the hostile bid, in 90 percent of the cases the deal is not closed if the target chooses to use a White knight as a defense tactic. A secondary objective with a defense tactic is to force the hostile bidder to increase the bid and pay more for the target company. In the Swedish market, the use of Corporate restructuring as a defense tactic has made the hostile bidder to increase the bid in 67 percent of the cases and the use of Positive public information has forced the hostile bidder to increase the bid in more than half of the cases.
The question why these defense tactics are the most frequently used strategies, is explained by two variables. The first one is the cost and simplicity variable, where Attack the logic of the bid and Public information ends up. These defense tactics are cost efficient and can be seen as natural step for the target company when deciding not to approve of the offer made by the acquirer. The second variable is the proven efficiency, where the target knows if implementing this defense tactic the risk of being acquired by the hostile bidder is relatively low, a good example of this is the White knight defense.
Supriatna, Asep K. "Optimal harvesting theory for predator-prey metapopulations /." Title page, contents and abstract only, 1998. http://web4.library.adelaide.edu.au/theses/09PH/09phs959.pdf.
Full textVan, Leeuwen Edwin. "Mathmatical Modelling of Predator-Multiple Prey Interactions." Thesis, Royal Holloway, University of London, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.499202.
Full textLerner, Thomas Ryan. "Modification of prey peptidoglycan by Bdellovibrio bacteriovorus." Thesis, University of Nottingham, 2012. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.631749.
Full textSiekmann, Ivo. "Mathematical modelling of pathogen-prey-predator interactions." München Verl. Dr. Hut, 2009. http://d-nb.info/99326039X/04.
Full textLondon, Josh M. "Harbor seals in Hood Canal : predators and prey /." Thesis, Connect to this title online; UW restricted, 2006. http://hdl.handle.net/1773/5394.
Full textGarza, Mark Isaac. "Predator induced defenses in prey with diverse predators." Texas A&M University, 2005. http://hdl.handle.net/1969.1/3309.
Full textHuggard, David John. "Prey selectivity of wolves in Banff National Park." Thesis, University of British Columbia, 1991. http://hdl.handle.net/2429/29880.
Full textScience, Faculty of
Zoology, Department of
Graduate
Pupovac-Velikonja, Ankica. "Environmental factors affecting predator-prey relationships among yeasts." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1999. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp01/MQ39869.pdf.
Full textDaiquin, Li. "Prey preferences of specialized jumping spiders (Araneae : Salticidae)." Thesis, University of Canterbury. Zoology, 1996. http://hdl.handle.net/10092/5867.
Full textAhlm, Kristoffer. "Prey specialization and diet of frogs in Borneo." Thesis, Umeå universitet, Institutionen för ekologi, miljö och geovetenskap, 2015. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-102020.
Full textWatt, Jon. "Prey selection by coastal otters (Lutra lutra L.)." Thesis, University of Aberdeen, 1991. http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=128373.
Full textLinkie, Matthew. "Tigers, prey loss and deforestation patterns in Sumatra." Thesis, University of Kent, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.405517.
Full textBotham, Marc Stephen. "Prey choice behaviour in three major Trinidadian piscovores." Thesis, University of Leeds, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.421976.
Full textJiang, Bin [Verfasser]. "Predators promote trait diversification in prey / Bin Jiang." Berlin : Freie Universität Berlin, 2018. http://d-nb.info/1169832156/34.
Full textKlepac, Petra. "Interacting populations : hosts and pathogens, prey and predators." Thesis, Massachusetts Institute of Technology, 2007. http://hdl.handle.net/1721.1/38995.
Full textIncludes bibliographical references.
The interactions between populations can be positive, neutral or negative. Predation and parasitism are both relationships where one species benefits from the interaction at the expense of the other. Predators kill their prey instantly and use it only for food, whereas parasites use their hosts both as their habitat and their food. I am particularly interested in microbial parasites (including bacteria, fungi, viri, and some protozoans) since they cause many infectious diseases. This thesis considers two different points in the population-interaction spectrum and focuses on modeling host-pathogen and predator-prey interactions. The first part focuses on epidemiology, i. e., the dynamics of infectious diseases, and the estimation of parameters using the epidemiological data from two different diseases, phocine distemper virus that affects harbor seals in Europe, and the outbreak of HIV/AIDS in Cuba. The second part analyzes the stability of the predator-prey populations that are spatially organized into discrete units or patches. Patches are connected by dispersing individuals that may, or may not differ in the duration of their trip. This travel time is incorporated via a dispersal delay in the interpatch migration term, and has a stabilizing effect on predator-prey dynamics.
by Petra Klepac.
Ph.D.
Bolohan, Noah. "Seasonal Variation in a Predator-Predator-Prey Model." Thesis, Université d'Ottawa / University of Ottawa, 2020. http://hdl.handle.net/10393/40899.
Full textJurcak, Ana M. "Defining the reaction space of predator-prey interactions." Bowling Green State University / OhioLINK, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1521461052087018.
Full textSogoni, Msimelelo. "The paradox of enrichment in predator-prey systems." University of Western Cape, 2020. http://hdl.handle.net/11394/7737.
Full textIn principle, an enrichment of resources in predator-prey systems show prompts destabilisation of a framework, accordingly, falling trophic communication, a phenomenon known to as the \Paradox of Enrichment" [54]. After it was rst genius postured by Rosenzweig [48], various resulting examines, including recently those of Mougi-Nishimura [43] as well as that of Bohannan-Lenski [8], were completed on this problem over numerous decades. Nonetheless, there has been a universal none acceptance of the \paradox" word within an ecological eld due to diverse interpretations [51]. In this dissertation, some theoretical exploratory works are being surveyed in line with giving a concise outline proposed responses to the paradox. Consequently, a quantity of di usion-driven models in mathematical ecology are evaluated and analysed. Accordingly, piloting the way for the spatial structured pattern (we denote it by SSP) formation in nonlinear systems of partial di erential equations [36, 40]. The central point of attention is on enrichment consequences which results toward a paradoxical state. For this purpose, evaluating a number of compartmental models in ecology similar to those of [48] will be of great assistance. Such displays have greater in uence in pattern formations due to diversity in meta-population. Studying the outcomes of initiating an enrichment into [9] of Braverman's model, with a nutrient density (denoted by n) and bacteria compactness (denoted by b) respectively, suits the purpose. The main objective behind being able to transform [9]'s system (2.16) into a new model as a result of enrichment. Accordingly, n has a logistic- type growth with linear di usion, while b poses a Holling Type II and nonlinear di usion r2 nb2 [9, 40]. Five fundamental questions are imposed in order to address and guide the study in accordance with the following sequence: (a) What will be the outcomes of introducing enrichment into [9]'s model? (b) How will such a process in (i) be done in order to change the system (2.16)'s stability state [50]? (c) Whether the paradox does exist in a particular situation or not [51]? Lastly, (d) If an absurdity in (d) does exist, is it reversible [8, 16, 54]? Based on the problem statement above, the investigation will include various matlab simulations. Therefore, being able to give analysis on a local asymptotic stability state when a small perturbation has been introduced [40]. It is for this reason that a bifurcation relevance comes into e ect [58]. There are principal de nitions that are undertaken as the research evolves around them. A study of quantitative response is presented in predator-prey systems in order to establish its stability properties. Due to tradeo s, there is a great likelihood that the growth rate, attack abilities and defense capacities of species have to be examined in line with reviewing parameters which favor stability conditions. Accordingly, an investigation must also re ect chances that leads to extinction or coexistence [7]. Nature is much more complex than scienti c models and laboratories [39]. Therefore, di erent mechanisms have to be integrated in order to establish stability even when a system has been under enrichment [51]. As a result, SSP system is modeled by way of reaction-di usion di erential equations simulated both spatially and temporally. The outcomes of such a system will be best suitable for real-world life situations which control similar behaviors in the future. Comparable models are used in the main compilation phase of dissertation and truly re ected in the literature. The SSP model can be regarded as between (2018-2011), with a stability control study which is of an original.
Halstead, Brian J. "Predator behavior and prey demography in patchy habitats." [Tampa, Fla] : University of South Florida, 2008. http://purl.fcla.edu/usf/dc/et/SFE0002414.
Full textTopham, Eric. "Biodiversity and ecosystem functioning in predator-prey communities." Thesis, University of Oxford, 2015. https://ora.ox.ac.uk/objects/uuid:c51b2a47-39bc-4b00-a749-5846ed75675d.
Full textLemos, Felipe de. "Spider mite web protects prey and predator alike." Universidade Federal de Viçosa, 2011. http://locus.ufv.br/handle/123456789/3958.
Full textConselho Nacional de Desenvolvimento Científico e Tecnológico
Em todo o mundo lavouras de tomate sofrem o ataque de pragas. Uma das principais pragas do tomate é o ácaro vermelho Tetranychus evansi Baker & Pritchard (Acari: Tetranychidae). Uma característica marcante de T. evansi é a sua alta produção de teia sobre suas plantas hospedeiras. Essa teia pode afetar diretamente os inimigos naturais, reduzindo a sua eficiência de predação ou indiretamente alterando seu comportamento de busca. No entanto, alguns ácaros predadores da família Phytoseiidae podem ser bem adaptados para lidar com a teia dos ácaros fitófagos. Para selecionar agentes de controle biológico eficientes é importante compreender as interações diretas e indiretas entre os organismos envolvidos no agroecossistema em questão. Nesta dissertação, foi investigado o papel da teia produzida por T. evansi como mediadora de interações diretas e indiretas com seus inimigos naturais. No Capítulo 1 foram investigados os efeitos da teia produzida por T. evansi em suas interações com o ácaro predador Phytoseiulus longipes Evans (Acari: Phytoseiidae). Foi avaliado se fêmeas de T. evansi reconhecem sinais químicos do predador e se estes sinais podem induzir os ácaros a produzirem mais teia. Os resultados mostram que a presa não produz mais teia em resposta a estímulos de risco de predação, no entanto, passa a depositar uma maior parcela de seus ovos suspensos na teia, longe da superfície da folha. Esses ovos suspensos sofreram uma menor predação por P. longipes do que os ovos que se encontravam na superfície da folha. Entretanto a taxa de predação de P. longipes sobre ovos de T. evansi em discos com e sem teia não diferiram, indicando que esse predador não é afetado negativamente pela teia de sua presa. No segundo capítulo foi estudado se a teia produzida por T. evansi pode afetar o comportamento de forragemamento de P. longipes modulando a sua preferência entre ambientes e presas. Estudou-se também se ocorre predação intraguilda entre P. longipes e outro ácaro predador Phytoseiulus macropilis (Banks) (Acari: Phytoseiidae), que podem coocorrerem sobre as mesmas plantas. Observou-se que P. longipes prefere as metades de discos de folhas que apresentavam uma estrutura mais complexa (mesmo quando eles não tinham alimento) em relação às metades dos discos com ovos e sem teia de T. evansi. Esta preferência por ambientes de estrutura complexa pode ser explicada pela menor taxa de predação intraguilda de P. macropilis observada em discos de tomate com teia de ácaros. A presença da teia reduziu a capacidade predatória de P. macropilis. A diferença entre ambos os predadores para lidar com a teia de ácaros fitófagos pode ser explicado em parte pelas diferenças no comprimento das setas dorsais j3, z2 e z4, que são mais longas em P. longipes. Com relação à preferência de P. longipes por espécies de presas, observou-se que os ácaros predadores escolheram T. evansi a T. urticae, tanto em presença quanto ausência de teia. Esses resultados indicam que a teia de T. evansi pode mediar o comportamento de forrageamento de ácaros da família Phytoseiidae de acordo com seus níveis de adaptações morfológicas e comportamentais. Em linhas gerais, pode-se concluir que os ácaros predadores P. longipes são bem adaptados para lidar com a grande quantidade de teia produzida por T. evansi. Além de não evitar plantas com elevada quantidade de teia, esse ácaro predador pode se beneficiar desse ambiente complexo, reduzindo a competição com outros predadores. No entanto, a presença do predador estimula T. evansi a mudar seu comportamento de oviposição, reduzindo a eficiência predatória de P. longipes. Assim, ao alterar o seu comportamento de oviposição em resposta aos sinais dos predadores, as fêmeas de T. evansi utilizam mais eficientemente sua teia para protegerem sua prole.
Worldwide, tomato suffers from herbivory. One of the most important tomato pests is the red spider mite Tetranychus evansi Baker & Pritchard (Acari: Tetranychidae). A striking characteristic of T. evansi is its high production of web over its host plants. The web can directly affect natural enemies by reducing its predation efficiency or indirectly by changing its foraging behaviour. However some Phytoseiidae can be well adapted to cope with spider mite webbing. To select efficient biologicol control agents, it is important to understand the direct and indirect interactions between the organims involved in the agroecosystem. In this dissertation, I investigated how the web produced by T. evansi mediates direct and indirect interactions with its natural enemies. In Chapter 1 I investigate the effects of the web produced by T. evansi on its interactions with the predatory mite Phytoseiulus longipes Evans. We tested whether spider mite females recognize predator cues and whether these can induce the spider mites to produce denser web. We found that the prey did not produce denser web in response to such cues, but laid more eggs suspended in the web, away from the leaf surface. These suspended eggs suffered less predation by P. longipes than eggs that were laid on the leaf surface, under the web. However the predation rate of P. longipes on eggs of T. evansi on discs with and without web was not different, indicating that this predatory mite is not negatively affected by the spider mite web. In the second Chapter I studied whether the complex web produced by spider mites could affect the foraging behaviour of P. longipes modulating its preference between patches and prey. Was also studied if there is intraguild predation between the predatory mites P. longipes and Phytoseiulus macropilis (Banks) (Acari: Phytoseiidae), which can co-occur on the same plants. We observed that P. longipes always preferred the leaf discs halves with more complex environmental structure (even when there was no food on it) to discs half with eggs and no web of T. evansi. The strong preference for patches with complex structure could be explained by the reduced rate of intraguild predation by P. macropilis observed on tomato discs with spider mite web. As observed, the presence of spider mite web reduced the predatory efficiency of P. macropilis in intraguild predation experiment. The difference between both predatory mites to cope with the web of spider mites could be explained in part by the differences in length of the setae j3, z2 and z4 that are longer in P. longipesi, but is needed manipulation of these traits. With respect to the preference of P. longipes by prey species, we observed that the predator chose T. evansi to T. urticae, both in the presence and absence of web. These results indicate that spider mite web can mediate the foraging behaviour of phytoseiid mites according to their level of morphological and behavioral adaptation to webbing. In general, we conclude that the predatory mite P. longipes is well adapted to cope with the higher web densities produced by T. evansi. Besides not avoid thus plants with high amounts of web, P. longipes can benefit from this complex environment by reducing competition with others predators. However the presence of the predatory mite stimulates T. evansi to change its oviposition behaviour, reducing the predation efficiency of P. longipes. Thus, by altering their oviposition behaviour in response to predator cues, females of T. evansi make better use of their web to protect their offspring.
Glaspie, Cassandra N. "Marine benthic predator-prey interactions and global change." W&M ScholarWorks, 2016. https://scholarworks.wm.edu/etd/1539616667.
Full textMurali, Suraj. "Reinforcement Learning for a Hunter and Prey Robot." Thesis, Uppsala universitet, Institutionen för informationsteknologi, 2018. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-389998.
Full textGo, Dong-Hun. "Three Essays in Economics of Prey-Predator Relation." DigitalCommons@USU, 2018. https://digitalcommons.usu.edu/etd/7031.
Full textDavison, Bruce. "Raptor communities in hill habitats in south-eastern Zimbabwe." Thesis, Rhodes University, 1998. http://hdl.handle.net/10962/d1005438.
Full textTruemper, Holly A. "Food habits and prey size-selection of yellow perch in extreme southern Lake Michigan, with emphasis on the prey : round goby." Virtual Press, 2003. http://liblink.bsu.edu/uhtbin/catkey/1260485.
Full textDepartment of Biology
Rowlands, William Llewelyn. "Is prey selection in young gadoids in the Irish Sea limited by gape size or by the spectrum of prey available?" Thesis, University of Liverpool, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.406715.
Full textDohet, Loïc. "Coevolution in the specific predator-prey system Rhizophagus grandis-Dendroctonus micans: with emphasis on the predator’s oviposition kairomones and prey symbioses." Doctoral thesis, Universite Libre de Bruxelles, 2016. http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/232990.
Full textRhizophagus grandis est un des rares exemples de prédateurs totalement spécifiques :présent en Europe et en Asie, il se nourrit exclusivement du scolyte Dendroctonus micans. Dans de telles associations, la coévolution prédateur-proie mène à la sélection de mécanismes d’évitement ou de résistance chez la proie, contre le prédateur. De précédentes observations en laboratoire ont suggéré que R. grandis pouvait pondre davantage d’œufs en présence de proies exotiques d’écologie comparable à celle de D. micans, mais qui n’auraient pu développer de résistance à l’encontre de ce prédateur, à l’instar des scolytes parasitiques nord-américains D. punctatus et D. valens. Il semble que la spécificité de l’association R. grandis-D. micans repose sur des signaux chimiques (kairomones) qui permettent au prédateur de repérer les galeries de sa proie et d’y ajuster le nombre d’œufs déposé à la quantité de larves de proies disponible. Néanmoins, on ignore encore la nature exacte des signaux régulant l’oviposition de R. grandis. Le fait que l’oviposition soit stimulée par des proies exotiques indique que la spécificité de cette association pourrait être limitée par des barrières géographiques. Contrairement à la plupart des scolytes qui tue des arbres ou s’attaque à des arbres mourants, D. micans se développe intégralement sur des arbres en bonne santé, en véritable parasite. Cette niche est fortement défendue par les composés toxiques de l’arbre (en particulier les terpènes), auxquels à la fois D. micans et R. grandis sont résistants. Certains insectes possèdent leurs propres processus de détoxification, mais ils peuvent également bénéficier de l’aide de microorganismes symbiotiques (bactéries et champignons). En comparaison avec les autres scolytes, les communautés microbiennes associées aux scolytes parasitiques est très peu documentée, comme dans le cas de D. micans et D. punctatus. En dehors de la détoxification, les symbiotes d’insectes peuvent contribuer à leur nutrition, les protéger contre des pathogènes, ou intervenir dans la communication chimique, ce qui affecte leurs hôtes comme les autres acteurs de la relation tritrophique arbre-scolyte-ennemi naturel. L’association R. grandis-D. micans est une opportunité unique d’étudier des aspects méconnus de la coévolution. Les objectifs de cette thèse étaient de :- (1) comparer le nombre d’œufs pondu par R. grandis sur sa proie spécifique, D. micans, et sur les proies exotiques D. punctatus et D. valens, afin de mettre en évidence de possibles résistances ;- (2) identifier les signaux chimiques qui régulent l’oviposition de R. grandis, et évaluer leur rôle dans la spécificité de l’association avec D. micans, en présence des proies exotiques D. punctatus et D. valens ;- (3) caractériser les communautés bactérienne et fongique associées aux populations parasitiques des scolytes D. micans, D. punctatus et D. valens, et investiguer comment ces microorganismes symbiotiques peuvent influencer leurs hôtes, selon leurs contraintes écologiques, ainsi que leurs ennemis naturels et arbres-hôtes. Nos résultats révèlent une oviposition équivalente de R. grandis en présence de la proie native D. micans et des proies exotiques D. punctatus et D. valens, ce qui illustre que la spécificité de cette association pourrait être limitée par des barrières géographiques mais ne met pas en évidence de possibles résistances à l’encontre du prédateur de longue date. Nous avons identifié des candidats robustes à la stimulation et à l’inhibition de la ponte de R. grandis, et leur rôle devrait être confirmé par des bioessais. Enfin, nous rapportons que la communauté microbienne associée aux populations parasitiques des scolytes D. micans, D. punctatus et D. valens est principalement constituée d’Entérobactéries et de levures répandues, et nous discutons des différentes façons dont ces symbiotes peuvent affecter leurs hôtes et autres acteurs de la relation tritrophique arbre-scolyte-ennemi naturel, selon leurs écologies respectives. Dans son ensemble, cette thèse souligne l’importance de considérer tous les niveaux de complexité biologique, des microorganismes associés aux proies jusqu’aux prédateurs, afin d’étudier des systèmes comme R. grandis-D. micans.
Doctorat en Sciences
info:eu-repo/semantics/nonPublished
Nizinski, Martha. "Caribbean spiny lobster and their molluscan prey: Are top-down forces key in structuring prey assemblages in a Florida Bay seagrass system." W&M ScholarWorks, 1998. https://scholarworks.wm.edu/etd/1539616795.
Full text