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Journal articles on the topic 'Temperature-adaptation'

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Published: 4 June 2021
Last updated: 11 February 2022

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1

KAMIHARA, Teijiro, and Midori YAMAMURA. "Temperature Adaptation in Yeast." JOURNAL OF THE BREWING SOCIETY OF JAPAN 87, no. 11 (1992): 773–79. http://dx.doi.org/10.6013/jbrewsocjapan1988.87.773.

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2

HAN Xu, 韩旭, 马军 MA Jun, 黎明 LI Ming, 付跃刚 FU Yue-gang, and 王加科 WANG Jia-ke. "Temperature adaptation of mapping camera." Optics and Precision Engineering 20, no. 6 (2012): 1175–81. http://dx.doi.org/10.3788/ope.20122006.1175.

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3

Bagriantsev, Sviatoslav N., and Elena O. Gracheva. "Molecular mechanisms of temperature adaptation." Journal of Physiology 593, no. 16 (January 5, 2015): 3483–91. http://dx.doi.org/10.1113/jphysiol.2014.280446.

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4

ENDO, Ayako, Mayumi SASAKI, Akihiko MARUYAMA, and Yasurou KURUSU. "Temperature Adaptation ofBacillus subtilisby ChromosomalgroELReplacement." Bioscience, Biotechnology, and Biochemistry 70, no. 10 (October 23, 2006): 2357–62. http://dx.doi.org/10.1271/bbb.50689.

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5

Rahmann, H. "Brain gangliosides and temperature adaptation." Cryobiology 25, no. 6 (December 1988): 557. http://dx.doi.org/10.1016/0011-2240(88)90437-3.

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6

Erdal, Ufuk G., Zeynep K. Erdal, and Clifford W. Randall. "ADAPTATION OF EBPR BACTERIA TO COLD TEMPERATURE THROUGH HOMEOVISCOUS ADAPTATION." Proceedings of the Water Environment Federation 2002, no. 15 (January 1, 2002): 145–59. http://dx.doi.org/10.2175/193864702784247675.

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7

Schoetter, Robert, David Grawe, Peter Hoffmann, Peter Kirschner, Angelika Grätz, and K. Heinke Schlünzen. "Impact of local adaptation measures and regional climate change on perceived temperature." Meteorologische Zeitschrift 22, no. 2 (April 1, 2013): 117–30. http://dx.doi.org/10.1127/0941-2948/2013/0381.

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8

Junttila, Olavi. "Plant adaptation to temperature and photoperiod." Agricultural and Food Science 5, no. 3 (May 1, 1996): 251–60. http://dx.doi.org/10.23986/afsci.72744.

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Plants respond to environmental conditions both by adaptation and by acclimation. The ability of the plants to grow, reproduce and survive under changing climatic conditions depends on the efficiency of adaptation and acclimation. The adaptation of developmental processes in plants to temperature and photoperiod is briefly reviewed. In annual plants this adaptation is related to growth capacity and to the timing of reproduction. In perennial plants growing under northern conditions, adaptation of the annual growth cycle to the local climatic cycle is of primary importance. Examples of the role of photothermal conditions in regulation of these phenological processes are given and discussed. The genetic and physiological bases for climatic adaptation in plants are briefly examined.
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9

Palonen, Eveliina, Miia Lindström, and Hannu Korkeala. "Adaptation of enteropathogenicYersiniato low growth temperature." Critical Reviews in Microbiology 36, no. 1 (January 20, 2010): 54–67. http://dx.doi.org/10.3109/10408410903382581.

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10

Chen, Tony H. H. "Plant adaptation to low temperature stress." Canadian Journal of Plant Pathology 16, no. 3 (September 1, 1994): 231–36. http://dx.doi.org/10.1080/07060669409500760.

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11

Aslanidi, K. B., D. P. Kharakoz, and L. M. Chailakhyan. "Temperature shock and adaptation in fish." Doklady Biochemistry and Biophysics 422, no. 1 (October 2008): 302–3. http://dx.doi.org/10.1134/s1607672908050128.

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12

Guschina, Irina A., and John L. Harwood. "Mechanisms of temperature adaptation in poikilotherms." FEBS Letters 580, no. 23 (June 30, 2006): 5477–83. http://dx.doi.org/10.1016/j.febslet.2006.06.066.

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13

Leroi, Armand M., Richard E. Lenski, and Albert F. Bennett. "EVOLUTIONARY ADAPTATION TO TEMPERATURE. III. ADAPTATION OFESCHERICHIA COLITO A TEMPORALLY VARYING ENVIRONMENT." Evolution 48, no. 4 (August 1994): 1222–29. http://dx.doi.org/10.1111/j.1558-5646.1994.tb05307.x.

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14

LIU Ju, 刘巨, 董得义 DONG De-yi, 辛宏伟 XIN Hong-wei, 李志来 LI Zhi-lai, 张学军 ZHANG Xue-jun, and 崔抗 CUI Kang. "Temperature adaptation of large aperture mirror assembly." Optics and Precision Engineering 21, no. 12 (2013): 3169–75. http://dx.doi.org/10.3788/ope.20132112.3169.

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15

Weifa, Zheng, and Tsing Chao-tsi. "High temperature adaptation of fresh water cyanobacterium." Journal of Lake Sciences 6, no. 4 (1994): 356–63. http://dx.doi.org/10.18307/1994.0409.

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16

BERRY, ELAINE D., and PEGGY M. FOEGEDING. "Cold Temperature Adaptation and Growth of Microorganisms†." Journal of Food Protection 60, no. 12 (December 1, 1997): 1583–94. http://dx.doi.org/10.4315/0362-028x-60.12.1583.

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Most microorganisms must accommodate a variety of changing conditions and stresses in their environment in order to survive and multiply. Because of the impact of temperature on all reactions of the cell, adaptations to fluctuations in temperature are possibly the most common. Widespread in the environment and well-equipped for cold temperature growth, psychrophilic and psychrotrophic microorganisms may yet make numerous adjustments when faced with temperatures lower than optimum. Phospholipid and fatty acid alterations resulting in increased membrane fluidity at lower temperatures have been described for many cold tolerant microorganisms while others may make no similar adjustment. While the enzymes of cold growing bacteria have been less extensively studied than those of thermophilic bacteria, it appears that function at low temperature requires enzymes with flexible conformational structure, in order to compensate for lower reaction rates. In many organisms, including psychrophilic and psychrotrophic bacteria, specific sets of cold shock proteins are induced upon abrupt shifts to colder temperatures. While this cold shock response has not been fully delineated, it appears to be adaptive, and may function to promote the expression of genes involved in translation when cells are displaced to lower temperatures. The cold shock response of Escherichia coli has been extensively studied, and the major cold shock protein CspA appears to be involved in the regulation of the response. Upon cold shock, the induction of CspA and its counterparts in most microorganisms studied is prominent, but transient; studies of this response in some psychrotrophic bacteria have reported constitutive synthesis and continued synthesis during cold temperature growth of CspA homologues, and it will be interesting to learn if these are common mechanisms of among cold tolerant organisms. Psychrotrophic microorganisms continue to be a spoilage and safety problem in refrigerated foods, and a greater understanding of the physiological mechanisms and implications of cold temperature adaptation and growth should enhance our ability to design more effective methods of preservation.
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17

WATANUKI, Shigeki. "Dark Adaptation Curve during Body Temperature Decrease." Annals of physiological anthropology 13, no. 1 (1994): 33–40. http://dx.doi.org/10.2114/ahs1983.13.33.

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18

Clarke, Andrew. "Costs and consequences of evolutionary temperature adaptation." Trends in Ecology & Evolution 18, no. 11 (November 2003): 573–81. http://dx.doi.org/10.1016/j.tree.2003.08.007.

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19

Caccuri, Anna Maria, Giovanni Antonini, Paolo Ascenzi, Maria Nicotra, Marzia Nuccetelli, Anna Paola Mazzetti, Giorgio Federici, Mario Lo Bello, and Giorgio Ricci. "Temperature Adaptation of GlutathioneS-Transferase P1–1." Journal of Biological Chemistry 274, no. 27 (July 2, 1999): 19276–80. http://dx.doi.org/10.1074/jbc.274.27.19276.

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20

Parsons, Peter A. "Animals and temperature: Phenotypic and evolution adaptation." Endeavour 21, no. 3 (January 1997): 135. http://dx.doi.org/10.1016/s0160-9327(97)80231-1.

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21

Ayupova, D. A., and O. A. Zabotina. "Plant oligosaccharides enhancing the low temperature adaptation." Biochemical Society Transactions 28, no. 5 (October 1, 2000): A400. http://dx.doi.org/10.1042/bst028a400b.

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22

Butler, Ethan E., and Peter Huybers. "Adaptation of US maize to temperature variations." Nature Climate Change 3, no. 1 (November 18, 2012): 68–72. http://dx.doi.org/10.1038/nclimate1585.

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23

Mitani, Yasuo, Ryo Futahashi, Zichao Liu, Xingcai Liang, and Yoshihiro Ohmiya. "Tibetan Firefly Luciferase with Low Temperature Adaptation." Photochemistry and Photobiology 93, no. 2 (November 3, 2016): 466–72. http://dx.doi.org/10.1111/php.12643.

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24

Gunderson, A. R., and J. H. Stillman. "An affinity for biochemical adaptation to temperature." Journal of Experimental Biology 217, no. 24 (December 15, 2014): 4273–74. http://dx.doi.org/10.1242/jeb.103192.

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25

Hartog, Jessica, Elif Dede, and Madhusudhan Govindaraju. "MapReduce framework energy adaptation via temperature awareness." Cluster Computing 17, no. 1 (May 25, 2013): 111–27. http://dx.doi.org/10.1007/s10586-013-0270-y.

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26

Chattopadhyay, M. K. "Mechanism of bacterial adaptation to low temperature." Journal of Biosciences 31, no. 1 (March 2006): 157–65. http://dx.doi.org/10.1007/bf02705244.

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27

Johnston, I. A., H. Guderley, C. E. Franklin, T. Crockford, and C. Kamunde. "ARE MITOCHONDRIA SUBJECT TO EVOLUTIONARY TEMPERATURE ADAPTATION?" Journal of Experimental Biology 195, no. 1 (October 1, 1994): 293–306. http://dx.doi.org/10.1242/jeb.195.1.293.

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Thermal tolerance and the respiratory properties of isolated red muscle mitochondria were investigated in Oreochromis alcalicus grahami from the alkaline hot-springs, Lake Magadi, Kenya. Populations of O. a. grahami were resident in pools at 42.8 °C and migrated into water reaching temperatures of 44.8 °C for short periods. The maximum respiration rates of mitochondria with pyruvate as substrate were 217 and 284 natom O mg-1 mitochondrial protein min-1 at 37 °C and 42 °C, respectively (Q10=1.71). Fatty acyl carnitines (chain lengths C8, C12 and C16), malate and glutamate were oxidised at 70­80 % of the rate for pyruvate. In order to assess evolutionary temperature adaptation of maximum mitochondrial oxidative capacities, the rates of pyruvate and palmitoyl carnitine utilisation in red muscle mitochondria were measured from species living at other temperatures: Notothenia coriiceps from Antarctica (-1.5 to +1 °C); summer-caught Myoxocephalus scorpius from the North Sea (10­15 °C); and Oreochromis andersoni from African lakes and rivers (22­30 °C). State 3 respiration rates had Q10 values in the range 1.8­2.7. At the lower lethal temperature of O. andersoni (12.5 °C), isolated mitochondria utilised pyruvate at a similar rate to mitochondria from N. coriiceps at 2.5 °C (30 natom O mg-1 mitochondrial protein min-1). Rates of pyruvate oxidation by mitochondria from M. scorpius and N. coriiceps were similar and were higher at a given temperature than for O. andersoni. At their normal body temperature (-1.2 °C), mitochondria from the Antarctic fish oxidised pyruvate at 5.5 % and palmitoyl-dl-carnitine at 8.8 % of the rates of mitochondria from the hot-spring species at 42 °C. The results indicate only modest evolutionary adjustments in the maximal rates of mitochondrial respiration in fish living at different temperatures.
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28

Mongold, Judith A., Albert F. Bennett, and Richard E. Lenski. "Evolutionary Adaptation to Temperature. IV. Adaptation of Escherichia coli at a Niche Boundary." Evolution 50, no. 1 (February 1996): 35. http://dx.doi.org/10.2307/2410778.

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29

Mongold, Judith A., Albert F. Bennett, and Richard E. Lenski. "EVOLUTIONARY ADAPTATION TO TEMPERATURE. IV. ADAPTATION OF ESCHERICHIA COLI AT A NICHE BOUNDARY." Evolution 50, no. 1 (February 1996): 35–43. http://dx.doi.org/10.1111/j.1558-5646.1996.tb04470.x.

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30

Basak, Surajit, Pamela Mukhopadhyay, Sanjib Kumar Gupta, and Tapash Chandra Ghosh. "Genomic adaptation of prokaryotic organisms at high temperature." Bioinformation 4, no. 8 (February 28, 2010): 352–56. http://dx.doi.org/10.6026/97320630004352.

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31

Steiner, K. C., and P. C. Berrang. "Microgeographic Adaptation to Temperature in Pitch Pine Progenies." American Midland Naturalist 123, no. 2 (April 1990): 292. http://dx.doi.org/10.2307/2426557.

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32

Kumar, Rakesh, Shelly Goomber, and Jagdeep Kaur. "Engineering lipases for temperature adaptation: Structure function correlation." Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics 1867, no. 11 (November 2019): 140261. http://dx.doi.org/10.1016/j.bbapap.2019.08.001.

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33

Berg, Kristel, Ingar Leiros, and Adele Williamson. "Temperature adaptation of DNA ligases from psychrophilic organisms." Extremophiles 23, no. 3 (March 2, 2019): 305–17. http://dx.doi.org/10.1007/s00792-019-01082-y.

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34

Pajoro, Alice, Leonie Verhage, and Richard G. H. Immink. "Plasticity versus Adaptation of Ambient–Temperature Flowering Response." Trends in Plant Science 21, no. 1 (January 2016): 6–8. http://dx.doi.org/10.1016/j.tplants.2015.11.015.

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35

Whiteley, N. M., E. W. Taylor, and A. J. El Haj. "Seasonal and latitudinal adaptation to temperature in crustaceans." Journal of Thermal Biology 22, no. 6 (December 1997): 419–27. http://dx.doi.org/10.1016/s0306-4565(97)00061-2.

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36

Van Doorslaer, Wendy, Robby Stoks, Cathy Duvivier, Anna Bednarska, and Luc De Meester. "POPULATION DYNAMICS DETERMINE GENETIC ADAPTATION TO TEMPERATURE INDAPHNIA." Evolution 63, no. 7 (July 2009): 1867–78. http://dx.doi.org/10.1111/j.1558-5646.2009.00679.x.

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37

Jones, A. L., A. C. Hann, J. L. Harwood, and D. Lloyd. "Temperature-induced membrane-lipid adaptation in Acanthamoeba castellanii." Biochemical Journal 290, no. 1 (February 15, 1993): 273–78. http://dx.doi.org/10.1042/bj2900273.

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A method has been developed for the separation of the major membrane fractions of Acanthamoeba castellanii after growth at different temperatures. The acyl-lipid compositions of individual membrane fractions, microsomal membranes, plasma membrane and mitochondria were analysed after a shift in culture temperature from 30 degrees C to 15 degrees C. The major change in lipid composition observed was an alteration in the relative proportions of oleate and linoleate. This reciprocal change was seen in all the membrane fractions, but occurred most rapidly in the phosphatidylcholine of the microsomal fraction. Thus, there appears to be a rapid induction of delta 12-desaturase activity in A. castellanii after a downward shift in growth temperature. Changes were also seen in the proportions of the n-6 C20 fatty acids, with a decrease in the proportions of icosadienoate and increases of icosatrienoate and arachidonate. However, unlike the alteration in oleate/linoleate ratios, this change was not seen in all the individual lipids of each membrane fraction.
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38

Buchumenski, Ilana, Osnat Bartok, Reut Ashwal-Fluss, Varun Pandey, Hagit T. Porath, Erez Y. Levanon, and Sebastian Kadener. "Dynamic hyper-editing underlies temperature adaptation in Drosophila." PLOS Genetics 13, no. 7 (July 26, 2017): e1006931. http://dx.doi.org/10.1371/journal.pgen.1006931.

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39

Salvadó, Z., F. N. Arroyo-López, J. M. Guillamón, G. Salazar, A. Querol, and E. Barrio. "Temperature Adaptation Markedly Determines Evolution within the GenusSaccharomyces." Applied and Environmental Microbiology 77, no. 7 (February 11, 2011): 2292–302. http://dx.doi.org/10.1128/aem.01861-10.

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ABSTRACTThe present study uses a mathematical-empirical approach to estimate the cardinal growth temperature parameters (Tmin, the temperature below which growth is no longer observed;Topt, the temperature at which the μmaxequals its optimal value; μopt, the optimal value of μmax; andTmax, the temperature above which no growth occurs) of 27 yeast strains belonging to differentSaccharomycesand non-Saccharomycesspecies.S. cerevisiaewas the yeast best adapted to grow at high temperatures within theSaccharomycesgenus, with the highest optimum (32.3°C) and maximum (45.4°C) growth temperatures. On the other hand,S. kudriavzeviiandS. bayanusvar.uvarumshowed the lowest optimum (23.6 and 26.2°C) and maximum (36.8 and 38.4°C) growth temperatures, respectively, confirming that both species are more psychrophilic thanS. cerevisiae. The remainingSaccharomycesspecies (S. paradoxus,S. mikatae,S. arboricolus, andS. cariocanus) showed intermediate responses. With respect to the minimum temperature which supported growth, this parameter ranged from 1.3 (S. cariocanus) to 4.3°C (S. kudriavzevii). We also tested whether these physiological traits were correlated with the phylogeny, which was accomplished by means of a statistical orthogram method. The analysis suggested that the most important shift in the adaptation to grow at higher temperatures occurred in theSaccharomycesgenus after the divergence of theS. arboricolus,S. mikatae,S. cariocanus,S. paradoxus, andS. cerevisiaelineages from theS. kudriavzeviiandS. bayanusvar.uvarumlineages. Finally, our mathematical models suggest that temperature may also play an important role in the imposition ofS. cerevisiaeversus non-Saccharomycesspecies during wine fermentation.
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40

Arnold, Kevin D., Jennifer Moye, and Gerald A. Winer. "Illusion versus reality: Children's understanding of temperature adaptation." Journal of Experimental Child Psychology 42, no. 2 (October 1986): 256–72. http://dx.doi.org/10.1016/0022-0965(86)90026-3.

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41

Zamir, D., and I. Gadish. "Pollen selection for low temperature adaptation in tomato." Theoretical and Applied Genetics 74, no. 5 (September 1987): 545–48. http://dx.doi.org/10.1007/bf00288849.

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42

Cruz, Luisa Ana B., Marit Hebly, Giang-Huong Duong, Sebastian A. Wahl, Jack T. Pronk, Joseph J. Heijnen, Pascale Daran-Lapujade, and Walter M. van Gulik. "Similar temperature dependencies of glycolytic enzymes: an evolutionary adaptation to temperature dynamics?" BMC Systems Biology 6, no. 1 (2012): 151. http://dx.doi.org/10.1186/1752-0509-6-151.

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43

Yang, Ling-Ling, Shu-Kun Tang, Ying Huang, and Xiao-Yang Zhi. "Low Temperature Adaptation Is Not the Opposite Process of High Temperature Adaptation in Terms of Changes in Amino Acid Composition." Genome Biology and Evolution 7, no. 12 (November 26, 2015): 3426–33. http://dx.doi.org/10.1093/gbe/evv232.

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44

Leroi, Armand M., Richard E. Lenski, and Albert F. Bennett. "Evolutionary Adaptation to Temperature. III. Adaptation of Escherichia coli to a Temporally Varying Environment." Evolution 48, no. 4 (August 1994): 1222. http://dx.doi.org/10.2307/2410380.

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45

Yamori, Wataru, Kouki Hikosaka, and Danielle A. Way. "Temperature response of photosynthesis in C3, C4, and CAM plants: temperature acclimation and temperature adaptation." Photosynthesis Research 119, no. 1-2 (June 26, 2013): 101–17. http://dx.doi.org/10.1007/s11120-013-9874-6.

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46

Kardol, Paul, Jonathan R. De Long, and David A. Wardle. "Local plant adaptation across a subarctic elevational gradient." Royal Society Open Science 1, no. 3 (November 2014): 140141. http://dx.doi.org/10.1098/rsos.140141.

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Predicting how plants will respond to global warming necessitates understanding of local plant adaptation to temperature. Temperature may exert selective effects on plants directly, and also indirectly through environmental factors that covary with temperature, notably soil properties. However, studies on the interactive effects of temperature and soil properties on plant adaptation are rare, and the role of abiotic versus biotic soil properties in plant adaptation to temperature remains untested. We performed two growth chamber experiments using soils and Bistorta vivipara bulbil ecotypes from a subarctic elevational gradient (temperature range: ±3 ° C) in northern Sweden to disentangle effects of local ecotype, temperature, and biotic and abiotic properties of soil origin on plant growth. We found partial evidence for local adaption to temperature. Although soil origin affected plant growth, we did not find support for local adaptation to either abiotic or biotic soil properties, and there were no interactive effects of soil origin with ecotype or temperature. Our results indicate that ecotypic variation can be an important driver of plant responses to the direct effects of increasing temperature, while responses to covariation in soil properties are of a phenotypic, rather than adaptive, nature.
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47

Dufourc, Erick J. "The role of phytosterols in plant adaptation to temperature." Plant Signaling & Behavior 3, no. 2 (February 2008): 133–34. http://dx.doi.org/10.4161/psb.3.2.5051.

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48

Suutari, M., K. Liukkonen, and S. Laakso. "Temperature adaptation in yeasts: the role of fatty acids." Journal of General Microbiology 136, no. 8 (August 1, 1990): 1469–74. http://dx.doi.org/10.1099/00221287-136-8-1469.

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49

Smrcka, Alan V., and Stan R. Szarek. "Phenotypical Temperature Adaptation of Protein Turnover in Desert Annuals." Plant Physiology 80, no. 1 (January 1, 1986): 206–10. http://dx.doi.org/10.1104/pp.80.1.206.

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50

Loladze, A., T. Druml, and C. R. Wellings. "Temperature adaptation in Australasian populations ofPuccinia striiformisf. sp. tritici." Plant Pathology 63, no. 3 (September 23, 2013): 572–80. http://dx.doi.org/10.1111/ppa.12132.

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