Academic literature on the topic 'Marine organisms sensitivity'
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Journal articles on the topic "Marine organisms sensitivity"
de Hoop, Lisette, Aafke M. Schipper, Rob S. E. W. Leuven, Mark A. J. Huijbregts, Gro H. Olsen, Mathijs G. D. Smit, and A. Jan Hendriks. "Sensitivity of Polar and Temperate Marine Organisms to Oil Components." Environmental Science & Technology 45, no. 20 (October 15, 2011): 9017–23. http://dx.doi.org/10.1021/es202296a.
Full textPutman, Nathan F., and Ruoying He. "Tracking the long-distance dispersal of marine organisms: sensitivity to ocean model resolution." Journal of The Royal Society Interface 10, no. 81 (April 6, 2013): 20120979. http://dx.doi.org/10.1098/rsif.2012.0979.
Full textMacLeod, Colin D., and Robert Poulin. "Parasitic infection: a buffer against ocean acidification?" Biology Letters 12, no. 5 (May 2016): 20160007. http://dx.doi.org/10.1098/rsbl.2016.0007.
Full textBennett, Scott, Carlos M. Duarte, Núria Marbà, and Thomas Wernberg. "Integrating within-species variation in thermal physiology into climate change ecology." Philosophical Transactions of the Royal Society B: Biological Sciences 374, no. 1778 (June 17, 2019): 20180550. http://dx.doi.org/10.1098/rstb.2018.0550.
Full textDeForest, David K., and Christian E. Schlekat. "Species sensitivity distribution evaluation for chronic nickel toxicity to marine organisms." Integrated Environmental Assessment and Management 9, no. 4 (May 28, 2013): 580–89. http://dx.doi.org/10.1002/ieam.1419.
Full textAraújo-Castro, Cristiane M. V., Lília P. Souza-Santos, Anny Gabrielle A. G. Torreiro, and Karina S. Garcia. "Sensitivity of the marine benthic copepod Tisbe biminiensis (copepoda, harpacticoida) to potassium dichromate and sediment particle size." Brazilian Journal of Oceanography 57, no. 1 (March 2009): 33–41. http://dx.doi.org/10.1590/s1679-87592009000100004.
Full textMcCormick, Lillian R., and Lisa A. Levin. "Physiological and ecological implications of ocean deoxygenation for vision in marine organisms." Philosophical Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences 375, no. 2102 (August 7, 2017): 20160322. http://dx.doi.org/10.1098/rsta.2016.0322.
Full textCanova, Luca, Michela Sturini, Federica Maraschi, Stefano Sangiorgi, and Elida Nora Ferri. "A Comparative Test on the Sensitivity of Freshwater and Marine Microalgae to Benzo-Sulfonamides, -Thiazoles and -Triazoles." Applied Sciences 11, no. 17 (August 25, 2021): 7800. http://dx.doi.org/10.3390/app11177800.
Full textDeidda, Irene, Roberta Russo, Rosa Bonaventura, Caterina Costa, Francesca Zito, and Nadia Lampiasi. "Neurotoxicity in Marine Invertebrates: An Update." Biology 10, no. 2 (February 18, 2021): 161. http://dx.doi.org/10.3390/biology10020161.
Full textBarry, John F., Matthew J. Turner, Jennifer M. Schloss, David R. Glenn, Yuyu Song, Mikhail D. Lukin, Hongkun Park, and Ronald L. Walsworth. "Optical magnetic detection of single-neuron action potentials using quantum defects in diamond." Proceedings of the National Academy of Sciences 113, no. 49 (November 22, 2016): 14133–38. http://dx.doi.org/10.1073/pnas.1601513113.
Full textDissertations / Theses on the topic "Marine organisms sensitivity"
Rodriguez, Dominguez Almendra. "How marine organisms cope with changing climate." Thesis, 2020. http://hdl.handle.net/2440/126088.
Full textThesis (Ph.D.) -- University of Adelaide, School of Biological Sciences, 2020
Book chapters on the topic "Marine organisms sensitivity"
Hummel, Herman, Roelof Bogaards, Tatiana Bek, Lennard Polishchuk, Claude Amiard-Triquet, Guy Bachelet, Michel Desprez, et al. "Sensitivity to stress in the bivalve Macoma balthica from the most northern (Arctic) to the most southern (French) populations: low sensitivity in Arctic populations because of genetic adaptations?" In Interactions and Adaptation Strategies of Marine Organisms, 127–38. Dordrecht: Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-017-1907-0_13.
Full textViarengo, A., B. Burlando, V. Evangelisti, S. Mozzone, and F. Dondero. "SENSITIVITY AND SPECIFICITY OF METALLOTHIONEIN AS A BIOMARKER FOR AQUATIC ENVIRONMENT BIOMONITORING." In Biomarkers in Marine Organisms, 29–43. Elsevier, 2001. http://dx.doi.org/10.1016/b978-044482913-9/50004-3.
Full textRiebesell, Ulf, and Philippe D. Tortell. "Effects of Ocean Acidification on Pelagic Organisms and Ecosystems." In Ocean Acidification. Oxford University Press, 2011. http://dx.doi.org/10.1093/oso/9780199591091.003.0011.
Full textRosenzweig, Cynthia, and Daniel Hillel. "Impacts of El Niño and La Niña Cycles: Systems and Sectors." In Climate Variability and the Global Harvest. Oxford University Press, 2008. http://dx.doi.org/10.1093/oso/9780195137637.003.0007.
Full textNavarro-Barranco, Carlos, Macarena Ros, José M. Tierno de Figueroa, and José M. Guerra-García. "Marine Crustaceans as Bioindicators: Amphipods as Case Study." In Fisheries and Aquaculture, 436–62. Oxford University Press, 2020. http://dx.doi.org/10.1093/oso/9780190865627.003.0017.
Full text"sequences allows for the design of PCR primer sets that specifically amplify the genes encoding the enzyme from DNA samples extracted from the natural environment (Henckel et al. 1999, Meyer et al. 1999, Mesarch et al. 2000). Although the PCR method is both specific and sensitive, such standard reactions are not quantitative. To obtain quantitative data from PCR-based analyses, statistical methods based on most probable number (MPN) estimations have been used (Wand et al. 1997). In MPN-PCR, DNA extracts are diluted before PCR amplification and limits are set on the number of genes in the sample by reference to known control dilutions. Another way to quantify PCR-amplified products for comparison is to include an internal control in the PCR reaction (Leser et al. 1995, Mesarch et al. 2000). Here, a known amount of target DNA is added to a PCR reaction containing DNA from the mixed microbial population. The known target DNA is complementary to the same primers and thus competes with the target sequences in the extracted DNA sample. By preparing a dilution series of the known and unknown DNA species, it is possible to quantify the amount of product produced from die complementary gene in the extracted DNA. The known DNA target can be generated by cloning the gene of interest or purifying the PCR-amplified product after which a deletion is introduced to give a differently sized PCR product. There exists many variations of the standard PCR technique. The sensitivity and specificity of the PCR may be improved by adopting a nested approach. The initial amplification is carried out with a pair of primers that are not organism-specific, whereafter a second round of amplification is conducted on the product using primers specific for an organism with target sites internal to the first primer pair (el Fantroussi et 1997, Levesque et al. 1997, Rheims and Stackebrandt 1999)." In Recent Advances in Marine Biotechnology, Vol. 8, 223. CRC Press, 2003. http://dx.doi.org/10.1201/9781482279986-16.
Full text"slowly growing natural populations. Various approaches have been adopted in order to improve the sensitivity. These have included the use of multiple probes labelled with a single fluor (Lee et al. 1993); or labelled with multiple fluors (Trebesius et al. 1994) and enzyme-linked probes or detection systems that allow signal amplification (Lebaron et al. 1997, Schonhuber et al. 1999). The latter indirect approach not only has the potential for signal amplification, but may also be used in natural samples showing high levels of autofluorescence. Any thorough identification method has to include positive and negative controls. False-positive results may either be caused by cells emitting autofluorescence upon excitation or by nonspecific binding of the probe to nontarget cells. Samples should therefore be checked for autofluorescence before hybridization and a negative control with a fluorescent oligonucleotide not complementary to rRNA has to be applied to check for sequence-independent nonspecific binding. Such non-specific binding may be due to interaction of the dye compound of the probe with hydrophobic cell components. Failures to detect cells containing target sequences (false-negatives) may originate from cells with either low cellular ribosome content or limited permeability of the cell periphery for the fluorescent probe (Manz et al. 1992). With the rapidly expanding database of 16S rRNA sequences, the problem of probe specificity has become more apparent and the design of probes is becoming increasingly difficult. These problems are also applicable to PCR and other oligonucleotide-dependent techniques. The problem of probe specificity may be overcome by using multiple specific oligonucleotide probes targeting different sites on the rRNA molecule and labelled with different fluorochromes. While a single oligonucleotide target sequence may be found in a number of related taxa, the probability that target sites for three designed oligonucleotides are found in a nontarget organism is, however, much reduced." In Recent Advances in Marine Biotechnology, Vol. 8, 232. CRC Press, 2003. http://dx.doi.org/10.1201/9781482279986-25.
Full textConference papers on the topic "Marine organisms sensitivity"
Ameryoun, Hamed, and Franck Schoefs. "Probabilistic Modeling of Roughness Effects Caused by Bio-Colonization on Hydrodynamic Coefficients: A Sensitivity Study for Jacket-Platforms in Gulf of Guinea." In ASME 2013 32nd International Conference on Ocean, Offshore and Arctic Engineering. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/omae2013-11101.
Full textSchoefs, Franck, and Hamed Ameryoun. "Probabilistic Modeling of the Bio-Colonization Effects on Hydrodynamic Forces With Several Combinations of Sea-State Condition: A Study on Jacket-Platforms in the Gulf of Guinea." In ASME 2013 32nd International Conference on Ocean, Offshore and Arctic Engineering. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/omae2013-11100.
Full textPistora, Vladislav, and Milan Brumovsky. "PTS Benchmark Performed Within IAEA Coordinated Research Project 9." In ASME 2009 Pressure Vessels and Piping Conference. ASMEDC, 2009. http://dx.doi.org/10.1115/pvp2009-77407.
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