Dissertations / Theses on the topic 'Seafood'
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Nguyen, Van Anh Wilson Norbert L. "Effects of food safety regulatory standards on seafood exports to US, EU and Japan." Auburn, Ala., 2009. http://hdl.handle.net/10415/1756.
Full textCOPPOLA, CHIARA. "SEAFOOD INSPECTION: CURRENT ISSUES." Doctoral thesis, Università degli Studi di Milano, 2020. http://hdl.handle.net/2434/784026.
Full textRagasa, Catherine. "Essays on food safety and competitiveness in the Philippine seafood industry." Diss., Connect to online resource - MSU authorized users, 2008.
Find full textTitle from PDF t.p. (viewed on July 23, 2009) Includes bibliographical references. Also issued in print.
van, der Meer Liesbeth. "Global revenues from wild seafood products." Thesis, University of British Columbia, 2012. http://hdl.handle.net/2429/42874.
Full textChan, Ho-pang, and 陳浩鵬. "Sustainable seafood certification in Hong Kong." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2011. http://hub.hku.hk/bib/B46733991.
Full textAlmojel, Suliman. "Characteristics of United States Seafood Consumers." UKnowledge, 2016. http://uknowledge.uky.edu/agecon_etds/38.
Full textRadhakrishnan, Sudhaharini. "Measurement of Thermal Properties of Seafood." Thesis, Virginia Tech, 1997. http://hdl.handle.net/10919/36834.
Full textMaster of Science
Stringer, Lawrence Jeffrey. "Modeling air transportation of fresh seafood." Thesis, Virginia Tech, 1990. http://hdl.handle.net/10919/42216.
Full textMaster of Science
Lyras, Ewgeniya. "Analýza organizační kultury společnosti SEAFOOD s.r.o." Master's thesis, Vysoká škola ekonomická v Praze, 2010. http://www.nusl.cz/ntk/nusl-16504.
Full textNicholas, Todd Andrew. "Antimicrobial Use of Native and Enzymatically Degraded Chitosans for Seafood Applications." Fogler Library, University of Maine, 2003. http://www.library.umaine.edu/theses/pdf/NicholasTA2003.pdf.
Full textLai, Chung-yin Stephanie. "Fish markets in Lei Yue Mun a means of waterfront development /." Click to view the E-thesis via HKUTO, 2009. http://sunzi.lib.hku.hk/hkuto/record/B43085635.
Full textChan, Hon-wing. "Food poisoning outbreaks in Hong Kong resulting from shellfish contamination /." Hong Kong : University of Hong Kong, 1996. http://sunzi.lib.hku.hk/hkuto/record.jsp?B17457762.
Full textNakamura, Katrina. "Sustainable seafood in an era of overfishing." Thesis, University of British Columbia, 2015. http://hdl.handle.net/2429/54907.
Full textGraduate and Postdoctoral Studies
Graduate
McDermott, Ryan. "Toward a more efficient seafood consumption advisory." Access to citation, abstract and download form provided by ProQuest Information and Learning Company; downloadable PDF file, 133 p, 2007. http://proquest.umi.com/pqdweb?did=1464121091&sid=17&Fmt=2&clientId=8331&RQT=309&VName=PQD.
Full textBernardi, C. E. M. "Seafood safety : a matter of any concern?" Doctoral thesis, Università degli Studi di Milano, 2009. http://hdl.handle.net/2434/148816.
Full textShaw, Brenda Jo. "Evaluation of risks to human health in Hong Kong from consumption of chemically contaminated seafood : a risk assessment approach /." Hong Kong : University of Hong Kong, 1995. http://sunzi.lib.hku.hk/hkuto/record.jsp?B14723657.
Full textTuuli, Cynthia Darta. "The croaker fishery and dried swimbladder trade in Hong Kong, and the reproductive biology of the greyfin croaker, Pennahia Anea." Thesis, Click to view the E-thesis via HKUTO, 2010. http://sunzi.lib.hku.hk/hkuto/record/B43778367.
Full textAmayo, Kenneth Osenewiwe. "Method development for identification and quantification of arsenolipids in seafood." Thesis, University of Aberdeen, 2013. http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=201887.
Full textGazzaz, Sahl Sadagah. "Parvalbumins in 21 common finfish species : presence and the effect of processing on immunoreactivity /." Thesis, Connect to this title online; UW restricted, 1992. http://hdl.handle.net/1773/5328.
Full textLau, Yuk-yee Sophia. "Seafood quality control and contamination in Hong Kong /." View the Table of Contents & Abstract, 2006. http://sunzi.lib.hku.hk/hkuto/record/B37120748.
Full textLau, Yuk-yee Sophia, and 劉玉兒. "Seafood quality control and contamination in Hong Kong." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2006. http://hub.hku.hk/bib/B45013536.
Full textFeliciano, Lizanel. "Shelf-life Extension of Seafood Using Sanitized Ice." The Ohio State University, 2009. http://rave.ohiolink.edu/etdc/view?acc_num=osu1252965039.
Full textDenton, Kristen E. "Effects of Facilitation Context on Attitude toward Sustainable Seafood." Thesis, California State University, Long Beach, 2018. http://pqdtopen.proquest.com/#viewpdf?dispub=10690032.
Full textThis study examined how adult guests to the California Science Center engage with a specific conservation education topic: sustainable seafood. Sustainable seafood is a common education message delivered in informal science institutions. This study also investigated whether engaging in an activity about sustainable seafood while simultaneously viewing live fish species would have a greater impact on guests than participating in the same activity while viewing a laboratory space.
The data showed that guests who participated in a hands-on activity about sustainable seafood knew more about conservation-related topics and were more likely to adopt behaviors conducive to sustainable seafood consumption than guests who participated in a different hands-on activity. The data also showed that the settings in which guests participate in this Sustainable Seafood activity do not influence their knowledge or behavior. This indicates that this Sustainable Seafood activity is effective in educating adult guests, regardless of the setting.
Grassiano, James W. "Wastewater treatment alternatives for a vegetable and seafood cannery." Thesis, This resource online, 1990. http://scholar.lib.vt.edu/theses/available/etd-06082009-170735/.
Full textNietes-Satapornvanit, Arlene. "Sustainable development of export-orientated farmed seafood in Thailand." Thesis, University of Stirling, 2014. http://hdl.handle.net/1893/20283.
Full textTetley, Sarah. "Why the Big 5? : understanding UK seafood consumer behaviour." Thesis, University of Kent, 2016. https://kar.kent.ac.uk/54790/.
Full textBeltramo, Dario. "Palytoxin and Okadaic acid as seafood contaminants: risk caracterization." Doctoral thesis, Università degli studi di Trieste, 2014. http://hdl.handle.net/10077/10374.
Full textThe increasing distribution of marine microalgae which may produce toxins poses concern on their possible accumulation in seafood, with possible toxic effects in humans after its consumption. Also in the Mediterranean Sea, microalgae producing okadaic acid (OA) and its analogues, the main diarrheic toxins contaminating edible shellfish, were frequently detected since several years. In addition, blooms of potentially toxic microalgae belonging to Ostreopsis genus, producing palytoxins (PLTXs), were also reported in the recent years. Simultaneously, PLTX and its analogue ovatoxin-a were identified in microalgal, shellfish and echinoderm samples. This phenomenon could represent a risk for human health since food borne intoxications, including some lethal cases, attributed to the consumption of seafood contaminated by palytoxin-like compounds, were reported in tropical areas. Furthermore, co-presence of microalgae producing OA and PLTXs and the possible consequent seafood contamination lead to consider the problem of toxic effects in humans due to a simultaneous exposure to both the toxins, which could induce synergistic effects. Thus, the aim of this study was to investigate the acute and short-term oral toxicity in mice by co-exposure to palytoxin and okadaic acid, in comparison to that of each single toxin. In particular, its aim is to identify not only the main toxic effects and the target organs, but also a NOAEL (No Observed Adverse Effect Level), useful in the assessment of subchronic toxicological risk, a situation that most likely corresponds to the toxin exposure by humans. The studies were carried out using female CD-1 mice (18-20 g body weight, 4 weeks old; Harlan Laboratories; S. Pietro al Natisone, Udine, Italy). All experiments were carried out at the University of Trieste, Italy in compliance with the Italian Decree n. 116/1992 as well as the EU Directive 2010/63/EU and the European Convention ETS 123. Initially, the effects of the acute oral administration of palytoxin (30, 90 and 270 g/kg) combined to OA (370 g/kg) were studied in comparison to those of the same doses of the single toxins. After gavage administration of the toxin or vehicle (phosphate buffered saline, containing 1.8 % ethanol; controls) to groups of 8 mice, the animals were monitored for 24 h (5 mice/dose) or 14 days (3 mice/dose) for symptoms. Aftr death or sacrifice, they were submitted to necropsy, taking also blood samples for hematochemical analysis and the main organs and tissues for the histological analysis by light microscopy. Within 24 h from the administration, toxic effects and lethality were recorded only in mice administered with the higher doses of PLTX (90 or 270 g/kg), alone or in combination with OA (370 g/kg). In addition, lethality was recorded only at the highest PLTX dose alone or combined with OA. The signs and symptoms recorded in mice (scratching, piloerection, abdominal swelling, ataxia, paralysis of the hind limbs, dyspnoea) were slightly more pronounced in mice administered with both the toxins with respect to those recorded in mice administered with PLTX alone. At 24 h from PLTX administration (90 or 270 g/kg), alone or with OA, necropsy showed redness and fluid accumulation in the small intestine and an increased liver weight, whereas histological analysis showed changes at the forestomach (slight ulcers and inflammation) and liver (reduced glycogen content). During the whole observation period, mice treated with the higher doses of PLTX, also combined with OA, showed a reduced body weight and food consumption, while no toxic effects were recorded after 14 days from the administration. Thus, the study showed a slight additive effect between PLTX and OA after acute oral administration, estimating a NOAEL of 30 g/kg for PLTX and 370 g/kg for OA in combination or as single toxins. Due to the lack of toxicity data on PLTX after repeated oral administration, a toxicity study on the toxin alone after its daily administration for 7 days was carried out. The toxin was administered to groups of 6 or 8 mice at four doses (3, 30, 90 or 180 g/kg/day) and the animals were observed up to 24 h after the last treatment or, for subgroups of 3 mice, up to 14 days. The toxin induced lethal and/or toxic effects at the dose of 30 g/kg/day and above, starting from the third day of treatment; some mice died also during the recovery period after the toxin administration. At these doses, a significant reduction of body weight, abdominal swelling, chromodacryorrhea, piloerection, dyspnoea, sedation and/or paralysis of the hind limbs were recorded during the treatment period. Necropsy revealed gastrointestinal changes (gastric ulcers and intestinal fluid) in mice died during the treatment period, while histological analysis showed lung inflammation, locally associated with necrosis, hypereosinophilia and separation of myocardial fibers and liver changes (reduced glycogen content and necrosis at the highest dose). These data allowed an estimation of a provisional NOAEL corresponding to 3 g/kg/day, with the evidence of a steep dose-response relationship. The last step of the research included the study of the toxic effects in mice induced by 7days oral administration of PLTX (3 and 10 g/kg/day) and OA (185 g/kg/day) association. Both the doses of PLTX combined to OA induced lethal effects, with signs or symptoms including scratching, dyspnoea, paralysis of the hind limbs and body weight loss. At 24 h from the last treatment, necropsy showed also the presence of fluid in the small intestine of mice administered with the highest dose of PLTX combined to OA, accompanied with a decreased liver weight. An effect on the liver was also evidenced by the increased transaminases serum levels and, in one mouse, by slight foci of necrosis, associated to thymus atrophy. On the contrary, no toxic effects were recorded after 14 days from the treatment, with the exception of a decreased body weight in mice administered with both PLTX doses combined to OA. Therefore, the study showed a slight potentiation of the toxic effects by the repeated oral co-exposure to PLTX and OA, which induced lethal and/or toxic effects that were not recorded after the administration of the single toxins. The overall results highlighted that the concomitant presence of palytoxin and okadaic acid, even if chemically different, could increase their toxicity profile and latent effects. Although no clearly evident synergic or additive effects were observed, they cannot be ruled out. The next steps would include a confirmatory study in a larger group of animals followed by a 14- and 28 day repeat dose study. Additional studies which may be useful in evaluating ‘true’ and realistic conditions of intoxications which should also include animal studies aimed to investigate the impact of age and of impairment of the gastrointestinal tract on the toxicity of seafood toxins. In addition, they should consider that the amount of contaminated seafood reported in the existing guidelines does not always represent the true amount ingested by the consumers, underlining the importance of assessing the exposure to low doses of toxins as done in these studies.
La crescente frequenza di proliferazioni di microalghe marine in grado di produrre tossine, pone il problema dell’accumulo di tali composti nei prodotti ittici, con possibili effetti tossici per l’uomo in seguito al loro consumo. Anche nel mare Mediterraneo, da anni viene rilevata la presenza di microalghe produttrici di acido okadaico (AO) e suoi analoghi, tossine diarroiche che possono contaminare i molluschi destinati all’alimentazione. Recentemente, si sono anche verificate anche proliferazioni di microalghe appartenenti al genere Ostreopsis, produttrici di palitossine). Contemporaneamente, nei campioni di microalghe, di molluschi ed echinodermi sono state rilevate la palitossina (PLTX) ed un suo analogo, l’ovatossina-a. Ciò pone il problema del rischio per l’uomo, poichè in aree tropicali sono state riportate intossicazioni alimentari, anche letali, attribuite all’assunzione di prodotti ittici contaminati da composti palitossino-simili. Inoltre, La co-presenza di alghe produttrici di palitossine e acido okadaico o loro analoghi, comporta una possibile contaminazione dei prodotti ittici, con effetti tossici nell’uomo conseguenti ad una co-esposizione ad entrambe le tossine e possibili effetti sinergici. Lo scopo della mia ricerca è stato pertanto quello di studiare la tossicità nel topo, acuta e a breve termine, conseguente alla co-esposizione orale alla palitossina e acido okadaico, in confronto a quella delle singole tossine, al fine di individuare gli effetti tossici principali e gli organi bersaglio, ma anche anche un NOAEL (No Observed Adverse Effect Level), da utilizzare per la valutazione del rischio subcronico, verosimilmente lo scenario più rispondente all’esposizione umana. Gli studi sono stati condotti su topi CD-1 di sesso femminile (18-20 g di peso corporeo, 4 settimane; Harlan Laboratories; S. Pietro al Natisone, Udine, Italia). Tutti gli esperimenti sono stati condotti presso l'Università di Trieste in conformità con il Decreto Italiano n. 116/1992, nonché la Direttiva 2010/63/UE dell'UE e la Convenzione europea ETS 123. Inizialmente, sono stati studiati gli effetti indotti dalla somministrazione acuta della palitossina (30, 90 e 270 µg/kg) in associazione con l’acido okadaico (370 µg/kg), rispetto a quelli indotti dalle stesse dosi delle singole tossine. In seguito alla somministrazione intragastrica delle tossine o del veicolo (soluzione salina tamponata con fosfato contenente l’1.8 % di etanolo; controlli) a gruppi di 8 topi, gli animali sono stati monitorati per 24 ore (5 topi/dose) o 14 giorni (3 topi/dose), registrando i sintomi e la sopravvivenza. Dopo il decesso o il sacrificio, è stato effettuato l’esame necroscopico, prelevando campioni ematici per l’analisi ematochimica ed i principali organi e tessuti per l’analisi istologica al microscopio ottico. Entro 24 ore dalla somministrazione, solo nei topi trattati con PLTX alle dosi maggiori (90 o 270 g/kg), singolarmente o con AO (370 g/kg), sono stati rilevati effetti tossici anche letali (letalità: 2/5 topi, in ogni gruppo). In seguito, effetti letali si sono verificati solo alla dose più alta di PLTX, singolarmente (1/3 topi, giorno 9) o con AO (2/3 topi, giorni 4 e 5). I sintomi ed i segni di tossicità (“scratching”, piloerezione, gonfiore addominale, atassia, paralisi agli arti inferiori e dispnea) erano lievemente più intensi nei topi trattati con entrambe le tossine rispetto a quelli dei topi trattati con la sola PLTX. Entro 24 ore dalla somministrazione della PLTX (90 o 270 g/kg), da sola o con l’AO, l’esame necroscopico ha rivelato arrossamento ed accumulo di liquido nell’intestino tenue ed un aumento ponderale del fegato, mentre l’analisi istologica ha evidenziato alterazioni gastriche (lievi ulcerazioni ed infiammazione allo stomaco non ghiandolare) ed epatiche (riduzione di glicogeno negli epatociti). Durante tutto il periodo di osservazione, nei topi trattati con le dosi più alte di PLTX, anche in combinazione con l’AO, sono stati inoltre rilevati un lieve calo del peso corporeo ed una lieve riduzione del consumo di cibo. Negli animali sopravvissuti fino a 14 giorni dal trattamento non sono state invece osservate alterazioni di rilievo. Lo studio ha così evidenziato un lieve effetto additivo tra PLTX ed AO dopo somministrazione acuta per via orale, stimando dei valori di NOAEL pari a 30 g/kg per la PLTX e 370 g/kg per l’AO, singolarmente o in combinazione. Vista la mancanza di studi di tossicità della PLTX dopo ripetute somministrazioni orali, prima di valutare gli effetti della sua somministrazione ripetuta con l’AO, è stato condotto uno studio di tossicità ripetuta sulla sola PLTX. Questa è stata somministrata a gruppi di 6 o 8 topi, una volta al giorno per 7 giorni, a quattro dosi (3, 30, 90 e 180 µg/kg/die). Gli animali sono stai osservati fino a 24 ore dall’ultimo trattamento e, sottogruppi di 3 topi, fino a 14 giorni. Il trattamento ha causato effetti letali e/o tossicità a partire dalla dose di 30 μg/kg/die, dal terzo giorno e, in alcuni casi, il decesso si è verificato durante il periodo di “recovery” in assenza di trattamento, indicando che gli effetti non sono totalmente reversibili. A tali dosi, durante il trattamento sono stati rilevati un significativo calo del peso corporeo, gonfiore addominale, cromodacriorrea, piloerezione, dispnea, sedazione e/o paralisi agli arti posteriori. Alterazioni macroscopiche gastrointestinali (ulcere gastriche e presenza di fluido intestinale) sono stati osservati nei topi morti durante il periodo di trattamento, mentre l’analisi istologica ha rilevato un’infiammazione polmonare, localmente associata a necrosi, iper-eosinofilia e separazione delle fibre nel miocardio ed alterazioni epatiche (ridotto contenuto in glicogeno e necrosi alla dose maggiore). Dai dati ottenuti è stato possibile calcolare un NOAEL “provvisorio” pari a 3 μg/kg/die, indicando una relazione dose-effetto piuttosto ripida. Sono stati quindi studiati gli effetti di 7 giorni di somministrazione con PLTX (3 e 10 g/kg/die) ed AO (185 g/kg/die), osservando che entrambe le dosi di PLTX associate con l’AO hanno causato effetti letali (1/8 topi a 3 g/kg/die ed 1/8 a 10 g /kg/die di PLTX in combinazione con l’AO/kg, nei giorni 7 e 8). Negli stessi gruppi, durante il periodo di trattamento gli animali avevano manifestato “scratching”, dispnea, paralisi agli arti posteriori e calo del peso corporeo. A 24 ore dall’ultimo trattamento, l’analisi necroscopica ha inoltre rivelato un accumulo di fluido nell’intestino tenue dei topi trattati con la dose maggiore di PLTX ed AO, accompagnato da un significativo calo ponderale del fegato. Un effetto a livello epatico è stato evidenziato anche da un incremento delle transaminasi sieriche e, in un topo, da lievi focolai di necrosi epatica, accompagnata da atrofia del timo. A 14 giorni dalla fine del trattamento non sono state invece rilevate significative alterazioni, eccetto un calo del peso corporeo degli animali trattati con l’associazione di AO e PLTX ad entrambe le dosi. Lo studio ha pertanto rivelato un potenziamento della tossicità da co-esposizione orale di PLTX ed AO, in grado di determinare effetti letali ed alterazioni non rilevabili dopo somministrazione delle singole tossine. I risultati complessivi hanno evidenziato che la presenza concomitante delle due tossine, benchè chimicamente differenti, potrebbe aumentare il loro profilo di tossicità esercitanto effetti latenti; anche se non sono stati osservati chiari effetti sinergici o additivi, questi non possono essere completamente esclusi. La caratterizzazione del rischio dovrebbe progredire con studi aventi un gruppo più ampio di animali ed un trattamento prolungato a 14/28 giorni ed oltre. Questi studi, mimando le condizioni alle quali avvengono le intossicazioni umane dovranno includere specifiche valutazioni volte ad indagare l'impatto del fattore età, del deterioramento del tratto gastrointestinale, della variabilità inter-individuale nonchè la possibile attività mutagena delle tossine. Inoltre, l’attuale legislazione dovrebbe essere rivista alla luce della reale quantità ingerita di molluschi da parte dei consumatori, sottolineando l'importanza della valutazione di dosi che producano intossicazioni non clinicamente evidenziabili, come effettuato in questi studi.
XXVI Ciclo
1978
Evason, David John. "Biochemical markers for storage abuse in raw black tiger prawns (Penaeus monodon)." Thesis, London South Bank University, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.312654.
Full textNorgren, Benjamin. "What role does aquaculture play in the global rise of antibiotic-resistant bacteria?" Thesis, Stockholms universitet, Institutionen för ekologi, miljö och botanik, 2020. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-182602.
Full textI en värld där den mänskliga befolkningen ökar krävs nya innovationer för att producera tillräckligt med mat. Vattenbrukets andel av den globala animaliska proteinproduktionen har ökat de senaste åren och kan ses som en potentiell lösning. Om vattenbruk dock hanteras ansvarslöst kan det uppstå negativa konsekvenser. En sådan konsekvens är utveckling av antibiotikaresistens hos skadliga bakterier. I denna litteraturstudie undersöker jag vattenbrukets påverkan på antibiotikaresistens genom att studera vad litteraturen säger om ackumulation av antibiotika i olika organismer och sediment, om antibiotika kan överföras till människor genom konsumtion av antibiotikabehandlade produkter, och om mänskliga patogener i vattenbruksodlingar kan förvärva antibiotikaresistens. Jag undersöker också vilka faktorer som bidrar till ansvarslös antibiotikaanvändning och hur den hanteras ur ett hållbarhetsperspektiv. Resultaten i denna studie tyder på att antibiotika kan ackumuleras i organismer och sediment men att det råder oklarheter huruvida konsumtion av antibiotikabehandlad mat påverkar mänskliga bakteriekulturer. Antibiotikaresistens kan dock överföras från antibiotikaresistenta bakterier till mänskliga patogener. Ansvarslös antibiotikaanvändning sker huvudsakligen i fattigare länder och det är förmodligen i stor utsträckning till följd av socioekonomiska faktorer som okunskap, fattigdom och livsmedelstrygghet. Slutligen föreslår jag lösningar som möjligen kan bidra till bättre hantering av framtida antibiotikaanvändning.
Brookmire, Lauren. "Optimization of the Quality and Safety of Cooked Seafood Products." Thesis, Virginia Tech, 2010. http://hdl.handle.net/10919/35180.
Full textStudies were performed to monitor the product heating profile during the baking and boiling of shrimp and the baking and pan-frying of salmon. Product color, texture, moisture content, mass loss, and pressed juice were evaluated during the cooking processes as the products reached the internal temperature recommended by the FDA. Studies were also performed on the inactivation of Salmonella cocktails in homogenized and non-homogenized shrimp and salmon. To effectively predict inactivation during cooking, the Bigelow, Fermi distribution, and Weibull distribution models were applied to the homogenized data. Minimum cooking temperatures necessary to destroy Salmonella sp. in shrimp and salmon were also determined. The heating profiles of the two products were modeled using the finite difference method. Temperature data directly from the modeled heating profiles was then used in the kinetic modeling of quality change and Salmonella inactivation during cooking.
It was concluded that consumers need to judge the doneness of both shrimp and Atlantic salmon by the lightness factor (CIE L*) of the core region of both products. The core regionâ s lightness factor, which a consumer may consider as opaqueness, more accurately represented the thermal doneness than the external qualities. The FDAâ s current recommendations for a 3 log reduction for intact seafood products and homogenized seafood products were each analyzed. Results were in agreement with the recommended 68°C plus 15 seconds for homogenized products. For intact products, shrimp inactivation results were in agreement with the recommended 63°C plus 15 seconds, but intact salmon achieved only a 2 log reduction by the temperature-time combination.
It was also found that predictive models can effectively describe the survival data for two Salmonella cocktails. The Weibull distribution model, which takes into account any tailing effect in survival data, fit the survival data of Salmonella in shrimp acceptably. The Fermi distribution model, which incorporates any shouldering effect in data, was an acceptable fit for the inactivation data for salmon.
Using three-dimensional slab geometry for salmon fillets and two-dimensional frustum cone geometry for shrimp resulted in acceptable model predictions of thermal distributions for the cooking methods studied. The temperature data attained directly from the modeled heating profiles was effectively used in the predictive quality and inactivation models. Agreeable first-order kinetic models were formulated for Î L and Î C color parameters in shrimp and salmon. Other kinetic models formulated were for texture change in salmon and pressed juice in both salmon and shrimp. Using a fixed inactivation level of 3 logs and a fixed quality of 95% best quality, optimal cooking conditions were determined that both provide a high quality product and assure microbial safety. Based on the specific cooking methods in this study, the optimal boiling times for extra jumbo and colossal sized shrimp were 100 seconds and 159 seconds, respectfully. The optimal oven baking times were 233 seconds for extra jumbo shrimp and 378 seconds for colossal shrimp. For Atlantic salmon, the optimal oven baking time was 1132 seconds and the optimal pan frying time was 399 seconds.
Master of Science
Nguyen, Thom Tien. "Attitude, motivation, and consumption of seafood in Bacninh province, Vietnam /." Tromsø : Norwegian College of Fishery Science, Universitetet i Tromsø, 2007. http://www.ub.uit.no/munin/bitstream/10037/1001/3/thesis.pdf.
Full textZhang, Wenbo. "Sustaining export-oriented value chains of farmed seafood in China." Thesis, University of Stirling, 2014. http://hdl.handle.net/1893/20347.
Full textAhmadov, Vugar. "Choice of a traceability strategy for U.S. seafood market enhancement : traceability as a signal of quality." Online access for everyone, 2006. http://www.dissertations.wsu.edu/Thesis/Fall2006/v_ahmadov_112906.pdf.
Full textLopata, Andreas L. "Identification and characterisation of specific allergens of Abalone (haliotis midae; mollusca) and other seafood species." Doctoral thesis, University of Cape Town, 1999. http://hdl.handle.net/11427/26929.
Full textTorén, Hanna. "Wild-caught seafood Swedish fisheries and consumption from a sustainability perspective." Thesis, Örebro universitet, Akademin för naturvetenskap och teknik, 2010. http://urn.kb.se/resolve?urn=urn:nbn:se:oru:diva-14331.
Full textLyver, André. "Formulation, shelf-life and safety studies on value-added seafood products." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1997. http://www.collectionscanada.ca/obj/s4/f2/dsk2/tape16/PQDD_0001/MQ29749.pdf.
Full textStella, Leonie. "Trawling deeper seas : the gendered production of seafood in Western Australia /." Access via Murdoch University Digital Theses Project, 1998. http://wwwlib.murdoch.edu.au/adt/browse/view/adt-MU20040913.155811.
Full textSwartz, Wilfram. "Five not so easy pieces : globalization of fishing and seafood markets." Thesis, University of British Columbia, 2013. http://hdl.handle.net/2429/44360.
Full textChironna, Serena. "Chasing Responsible Sourcing: The case of UK retailers and sustainable seafood." Thesis, Uppsala universitet, Institutionen för geovetenskaper, 2016. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-302824.
Full textJonell, Malin. "Kind of turquoise : Effects of seafood eco-certification and sustainable consumption." Doctoral thesis, Stockholms universitet, Institutionen för ekologi, miljö och botanik, 2016. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-132676.
Full textAt the time of the doctoral defense, the following paper was unpublished and had a status as follows: Paper 5: Manuscript.
Mansfield, Becky K. "Globalizing nature : political and cultural economy of a global seafood industry /." view abstract or download file of text, 2001. http://wwwlib.umi.com/cr/uoregon/fullcit?p3018380.
Full textTypescript. Includes vita and abstract. Includes bibliographical references (leaves 143-163). Also available for download via the World Wide Web; free to University of Oregon users.
Phan, Thanh Lam. "Sustainable development of export-orientated farmed seafood in Mekong Delta, Vietnam." Thesis, University of Stirling, 2014. http://hdl.handle.net/1893/20752.
Full textStella, Leonie C. "Trawling deeper seas: the gendered production of seafood in Western Australia." Thesis, Stella, Leonie C. (1998) Trawling deeper seas: the gendered production of seafood in Western Australia. PhD thesis, Murdoch University, 1998. https://researchrepository.murdoch.edu.au/id/eprint/346/.
Full textStella, Leonie C. "Trawling Deeper Seas: the Gendered Production of Seafood in Western Australia." Murdoch University, 1998. http://wwwlib.murdoch.edu.au/adt/browse/view/adt-MU20040913.155811.
Full textDel, Favero Giorgia. "Characterization of the risk of palytoxin and analogues as seafood contaminants." Doctoral thesis, Università degli studi di Trieste, 2012. http://hdl.handle.net/10077/7354.
Full textThe present thesis was developed for the characterization of the risk associated to palytoxins as seafood contaminants. To this aim, an integrated approach between in vitro and in vivo studies was chosen. Palytoxin and its analogues are known seafood contaminants that can accumulate in several edible species of shellfish, fish, crustaceans and echinoderms. Generally, primary symptoms associated to the ingestion of contaminated food involve the gastro-intestinal apparatus and later develop with the involvement of the muscular tissue. For a better comprehension of the mechanism of action of this family of biotoxins, the effects of PLTX have been studied on primary culture of mouse skeletal muscle cells. The myotoxic insult triggered by PLTX was described in detail with the definition of the cytotoxicity together with the description of the morphologic alterations and functional impairment caused by the toxin. Moreover, the influence of the ionic composition of the extracellular medium on the effects of the toxin was elucidated. Primary cultures of skeletal muscle cells, that presents in vitro many of the peculiarities of the adult muscle fiber, allowed the investigation of the membrane mechanisms that regulate the intracellular calcium increase triggered by the toxin. It was possible to discriminate the difference between calcium release from intracellular stores and the calcium entrance from extracellular compartment both elicited by the toxin, and to understand the importance of the latter in relation to the toxic event. Moreover, the involvement of the main membrane channels and transporters that may be related to the entrance of calcium was investigated and the crucial role of stretch-activated channels in the mechanism of toxicity was demonstrated. Once defined the crucial molecular mechanisms of action of PLTX, experiments were also performed with two of its analogue: the 42-hydroxyl-palytoxin and the ostreocin-D. In parallel to in vitro studies, the effects of repeated oral administration of PLTX in mice were also investigated. In fact, in vitro studies are not sufficient for the complete comprehension of the real hazard associated to a food contaminant, since molecules once in contact with the body may undergo adsorption, distribution and metabolism before reaching the target tissue. Short-term (7 days) administration of the toxin revealed toxicity at all the doses tested and lethality was recorded in the treated animals already from the dose of 30 µg/kg. Histological analysis highlighted alterations in several tissues: severe inflammatory processes and even foci of necrosis were observed in lungs. Alteration of the muscular tissues was visible as fiber separation and degeneration in the heart and increased cellularity between fibers in skeletal muscle. Moreover, depletion of glycogen content of hepatocytes and moderate alterations of the spleen were also observed. Data collected in the present project revealed, for the first time, toxicity of PLTX at doses much lower than that currently used by European Food Safety Authority (EFSA) for the estimation of limit values for presence of these compounds in seafood. For this reason, these results are likely to have a considerable impact at regulatory level and to have crucial importance for the protection of the consumers.
Il presente lavoro di tesi è stato sviluppato con lo scopo di caratterizzare il rischio associato alla presenza delle palitossine quali contaminanti dei prodotti ittici destinati ad uso alimentare. A tal fine, è stato scelto un approccio integrato tra studi in vitro e in vivo. La palitossina e i suoi analoghi sono noti contaminanti dei prodotti ittici e possono accumularsi in diverse specie edibili di molluschi, pesci, crostacei ed echinodermi. Generalmente, i primi sintomi associati all’ingestione di cibo contaminato coinvolgono l’apparato gastro-intestinale e poi si sviluppano con l’interessamento del tessuto muscolare. Per una migliore comprensione del meccanismo d’azione di questa famiglia di biotossine, gli effetti della PLTX sono stati studiati mediante colture primarie murine di cellule muscolari scheletriche. L’insulto miotossico indotto dalla PLTX è stato descritto nel dettaglio con la definizione della citotossicità assieme alla descrizione delle modifiche morfologiche e delle alterazioni funzionali causate dalla tossina. Inoltre, è stata caratterizzata l’influenza della composizione ionica dell’ambiente extracellulare negli effetti della tossina. Le colture primarie di cellule muscolari scheletriche, che presentano molte delle caratteristiche peculiari della fibra muscolare adulta, hanno permesso l’indagine dei meccanismi che regolano l’aumento intracellulare di calcio indotto dalla tossina. E’ stato possibile discriminare la differenza tra il rilascio di calcio dai depositi intracellulari e l’entrata di calcio dai compartimenti extracellulari, entrambi effetti indotti dalla tossina, e comprendere l’importanza del secondo meccanismo in relazione agli eventi tossici. E’ stato indagato il coinvolgimento dei canali e trasportatori di membrana in relazione all’ingresso di calcio ed è stato dimostrato il ruolo cruciale dei canali attivati da stiramento nel meccanismo di tossicità. Una volta definiti i meccanismi d’azione cruciali per la PLTX, esperimenti sono stati condotti anche con due dei suoi analoghi, la 42-idrossi-palitossina e l’ostreocina-D. Parallelamente agli studi in vitro, sono stati studiati gli effetti della somministrazione orale ripetuta della PLTX nel topo. Infatti, gli studi in vitro non sono sufficienti alla comprensione del reale pericolo associato ad un contaminate alimentare, dal momento che, le molecole, una volta a contatto con l’organismo, possono subire assorbimento, distribuzione e metabolismo prima di raggiungere il tessuto bersaglio. La somministrazione a breve termine della tossina (7 giorni) ha rivelato tossicità a tutte le dosi somministrate, e letalità è stata registrata negli animali trattati già alla dose di 30 µg/kg. Le analisi istologiche hanno evidenziato alterazioni a carico di diversi tessuti: a livello polmonare sono stati osservati severi processi infiammatori associati anche a focolai di necrosi. Le alterazioni del tessuto muscolare erano visibili come degenerazione e separazione delle fibre nel cuore e aumento degli elementi cellulari tra le fibre del muscolo scheletrico. Inoltre sono stai osservati, deplezione del contenuto di glicogeno negli epatociti e moderate alterazioni della milza. I dati raccolti nel presente elaborato hanno rivelato, per la prima volta, la tossicità della palitossina a dosi molto inferiori rispetto a quelle correntemente utilizzate della European Food Safety Authority (EFSA) per la stima di valori limite per la presenza di questi composti nei prodotti ittici destinati ad uso alimentare. Per questo motivo, i risultati avranno probabilmente un considerevole impatto a livello legislativo e un’importanza cruciale per la protezione dei consumatori.
XXIV Ciclo
1984
De, Aguiar Saldanha Pinheiro Ana Cristina <1978>. "Optimization of emerging treatments for seafood products and by-products valorization." Doctoral thesis, Alma Mater Studiorum - Università di Bologna, 2022. http://amsdottorato.unibo.it/10147/1/De%20Aguiar_PhD%20Thesis.pdf.
Full textJosephson, David Brian. "Mechanisms for the formation of volatiles in fresh seafood flavors." 1987. http://catalog.hathitrust.org/api/volumes/oclc/15646794.html.
Full textWu, Tien-Hsiang, and 吳天祥. "Evaluating Taiwan seafood traceability system." Thesis, 2007. http://ndltd.ncl.edu.tw/handle/87977029049051405812.
Full text國立臺灣海洋大學
應用經濟研究所
95
This investigation into the traceability baseline in Taiwan finds that private sector seafood firms have developed a substantial capacity to trace. Traceability systems are a tool to help firms manage the flow of inputs and products to improve efficiency, product differentiation, food safety, and products quality. Firms balance the private costs and benefits of traceability to determine the efficient level of traceability. It has developed a number of mechanisms to correct the problem, including contracting, third-party safety/quality audits, and good practices. The best targeted government polices for strengthening firms’ incentives to invest in traceability are aimed at ensuring that unsafe or falsely advertised foods are quickly removed form the system, while allowing firms the flexibility to determine the manner. Possible policy tools include timed recall standards, increased penalties for distribution of unsafe seafoods and increased foodborne-illness surveillance. The cost of implementation of traceability systems is likely to vary enormously between business and sectors depending on the type of technology adopted, the amount of information required to be stored and the complexity of the seafood chain. It is clear that traceability comes at a cost. But the costs of not having it, or having inefficient systems in pace may be severe both for governments, consumers, individual companies and the food industry as a whole.
Sykes, Stephen James. "Engineering aspects of seafood refrigeration." Thesis, 1987. https://eprints.utas.edu.au/22307/1/whole_SykesStephenJames1988_thesis.pdf.
Full textLiew, Sher Lee, and 劉雪麗. "Study of Factors Affecting Glazing of Frozen Seafood and Shelf Life Prediction of Short Shelf Life Seafood." Thesis, 2017. http://ndltd.ncl.edu.tw/handle/p7ajk5.
Full text國立臺灣海洋大學
食品科學系
105
Glazing, as a quality protecting tool, has a long history and a common practice in frozen seafood processing. The aim of this study is to investigate “can this procedure re-define and extend shelf-life for seafood food which has limited shelf-life, e.g. within 3 months?” Criteria for glazing practice include surface/weight ratio, dipping time, and dipping cycle. Three species and processing types, salmon fillet, halibut fillet, and capelin whole fish, varied mainly by their lipid contents, were selected and quality index, TRARS, TVB-N, and drip-loss were used to evaluate their quality changes during normal, -25℃, and accelerated storage test, at -15℃ and -5℃ up to 12 weeks. Results indicated, the highest glazing pick-up rate can be achieved at smaller surface area, thinner, and longer dipping time. However, there are no significant difference in pick-up rate between second and third glazing cycles. Hence, a reference glazing table was developed indicating the suitable practice to achieve the target glazing pick-up ratio. Glazing pick-up ratio were set at 0% (control),15% and 30% for fish samples. During 12 weeks’ storage period, gradually but significantly increased TBARS and TVB-N were observed for all treatments, while there was no significant difference among drip-loss changes. Arrhenius equation was used to calculate the activation energy (Ea) for TBARS and TVB-N of the tested samples which were then used to predict the expected shelf-life of these short shelf-life products. Results suggested that TBARS is a better quality index for high-fat fish, such as salmon in this study, while TVB-N is a more suitable index for low-fat or smaller whole fish. Results showed that smaller area-weight ratio, the more glaze uptake. 15% glazed is adequate and effective to guarantee the final quality of higher fat fish samples (>20%) during frozen storage. Excessive glazing (>15%) will have the adverse effect on the quality changes due to longer time exposure to higher environmental temperature.