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1

Kassen, Rees. "Experimental Evolution of Innovation and Novelty." Trends in Ecology & Evolution 34, no. 8 (2019): 712–22. http://dx.doi.org/10.1016/j.tree.2019.03.008.

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2

Muller, G. B., and G. P. Wagner. "Novelty in Evolution: Restructuring the Concept." Annual Review of Ecology and Systematics 22, no. 1 (1991): 229–56. http://dx.doi.org/10.1146/annurev.es.22.110191.001305.

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3

Gomes, Jorge, Pedro Mariano, and Anders Lyhne Christensen. "Novelty-Driven Cooperative Coevolution." Evolutionary Computation 25, no. 2 (2017): 275–307. http://dx.doi.org/10.1162/evco_a_00173.

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Abstract (sommario):
Cooperative coevolutionary algorithms (CCEAs) rely on multiple coevolving populations for the evolution of solutions composed of coadapted components. CCEAs enable, for instance, the evolution of cooperative multiagent systems composed of heterogeneous agents, where each agent is modelled as a component of the solution. Previous works have, however, shown that CCEAs are biased toward stability: the evolutionary process tends to converge prematurely to stable states instead of (near-)optimal solutions. In this study, we show how novelty search can be used to avoid the counterproductive attracti
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Streelman, Jeffrey Todd, and R. Craig Albertson. "Evolution of novelty in the cichlid dentition." Journal of Experimental Zoology Part B: Molecular and Developmental Evolution 306B, no. 3 (2006): 216–26. http://dx.doi.org/10.1002/jez.b.21101.

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5

Aboobaker, Aziz, and Mark Blaxter. "Hox gene evolution in nematodes: novelty conserved." Current Opinion in Genetics & Development 13, no. 6 (2003): 593–98. http://dx.doi.org/10.1016/j.gde.2003.10.009.

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6

Rebeiz, Mark, and Miltos Tsiantis. "Enhancer evolution and the origins of morphological novelty." Current Opinion in Genetics & Development 45 (August 2017): 115–23. http://dx.doi.org/10.1016/j.gde.2017.04.006.

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7

Bush, Stephen J., Lu Chen, Jaime M. Tovar-Corona, and Araxi O. Urrutia. "Alternative splicing and the evolution of phenotypic novelty." Philosophical Transactions of the Royal Society B: Biological Sciences 372, no. 1713 (2017): 20150474. http://dx.doi.org/10.1098/rstb.2015.0474.

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Alternative splicing, a mechanism of post-transcriptional RNA processing whereby a single gene can encode multiple distinct transcripts, has been proposed to underlie morphological innovations in multicellular organisms. Genes with developmental functions are enriched for alternative splicing events, suggestive of a contribution of alternative splicing to developmental programmes. The role of alternative splicing as a source of transcript diversification has previously been compared to that of gene duplication, with the relationship between the two extensively explored. Alternative splicing is
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8

Charlesworth, B. "EVOLUTION: On the Origins of Novelty and Variation." Science 310, no. 5754 (2005): 1619–20. http://dx.doi.org/10.1126/science.1119727.

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9

Benkman, Craig W., and Anna K. Lindholm. "The advantages and evolution of a morphological novelty." Nature 349, no. 6309 (1991): 519–20. http://dx.doi.org/10.1038/349519a0.

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10

Markov, Gabriel V., and Ralf J. Sommer. "The Evolution of Novelty in Conserved Gene Families." International Journal of Evolutionary Biology 2012 (June 19, 2012): 1–8. http://dx.doi.org/10.1155/2012/490894.

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One of the major aims of contemporary evolutionary biology is the understanding of the current pattern of biological diversity. This involves, first, the description of character distribution at various nodes of the phylogenetic tree of life and, second, the functional explanation of such changes. The analysis of character distribution is a powerful tool at both the morphological and molecular levels. Recent high-throughput sequencing approaches provide new opportunities to study the genetic architecture of organisms at the genome-wide level. In eukaryotes, one overarching finding is the absen
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11

Sumner, Seirian. "The importance of genomic novelty in social evolution." Molecular Ecology 23, no. 1 (2013): 26–28. http://dx.doi.org/10.1111/mec.12580.

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12

Gomes, Jorge, Paulo Urbano, and Anders Lyhne Christensen. "Evolution of swarm robotics systems with novelty search." Swarm Intelligence 7, no. 2-3 (2013): 115–44. http://dx.doi.org/10.1007/s11721-013-0081-z.

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13

Lehman, Joel, and Kenneth O. Stanley. "Abandoning Objectives: Evolution Through the Search for Novelty Alone." Evolutionary Computation 19, no. 2 (2011): 189–223. http://dx.doi.org/10.1162/evco_a_00025.

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In evolutionary computation, the fitness function normally measures progress toward an objective in the search space, effectively acting as an objective function. Through deception, such objective functions may actually prevent the objective from being reached. While methods exist to mitigate deception, they leave the underlying pathology untreated: Objective functions themselves may actively misdirect search toward dead ends. This paper proposes an approach to circumventing deception that also yields a new perspective on open-ended evolution. Instead of either explicitly seeking an objective
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14

Arnqvist, Göran. "Editorial rejects? Novelty, schnovelty!" Trends in Ecology & Evolution 28, no. 8 (2013): 448–49. http://dx.doi.org/10.1016/j.tree.2013.05.007.

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15

Soltis, P. S. "Hybridization, speciation and novelty." Journal of Evolutionary Biology 26, no. 2 (2013): 291–93. http://dx.doi.org/10.1111/jeb.12095.

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16

Stipp, Horst. "The Evolution of Neuromarketing Research: From Novelty to Mainstream." Journal of Advertising Research 55, no. 2 (2015): 120–22. http://dx.doi.org/10.2501/jar-55-2-120-122.

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17

Renwick, Douglas W. S., Dermot Breslin, and Ilfryn Price. "Nurturing Novelty: Toulmin's Greenhouse, Journal Rankings and Knowledge Evolution." European Management Review 16, no. 1 (2018): 167–78. http://dx.doi.org/10.1111/emre.12334.

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18

Baldus, Bernd. "Contingency, novelty and choice. Cultural evolution as internal selection." Journal for the Theory of Social Behaviour 45, no. 2 (2014): 214–37. http://dx.doi.org/10.1111/jtsb.12065.

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19

Moczek, Armin P. "On the origins of novelty in development and evolution." BioEssays 30, no. 5 (2008): 432–47. http://dx.doi.org/10.1002/bies.20754.

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20

Xia, Xuewen, Lei Tong, Yinglong Zhang, et al. "NFDDE: A novelty-hybrid-fitness driving differential evolution algorithm." Information Sciences 579 (November 2021): 33–54. http://dx.doi.org/10.1016/j.ins.2021.07.082.

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21

Nijhout, H. Frederik, and Kenneth Z. McKenna. "The Origin of Novelty Through the Evolution of Scaling Relationships." Integrative and Comparative Biology 57, no. 6 (2017): 1322–33. http://dx.doi.org/10.1093/icb/icx049.

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22

Nichols, Paul, Martin J. Genner, Cock van Oosterhout, et al. "Secondary contact seeds phenotypic novelty in cichlid fishes." Proceedings of the Royal Society B: Biological Sciences 282, no. 1798 (2015): 20142272. http://dx.doi.org/10.1098/rspb.2014.2272.

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Abstract (sommario):
Theory proposes that genomic admixture between formerly reproductively isolated populations can generate phenotypic novelty for selection to act upon. Secondary contact may therefore be a significant promoter of phenotypic novelty that allows species to overcome environmental challenges and adapt to novel environments, including during adaptive radiation. To date, this has largely been considered from the perspective of interspecific hybridization at contact zones. However, it is also possible that this process occurs more commonly between natural populations of a single species, and thus its
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23

Erwin, Douglas H. "Developmental capacity and the early evolution of animals." Journal of the Geological Society 178, no. 5 (2021): jgs2020–245. http://dx.doi.org/10.1144/jgs2020-245.

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Disentangling the factors underlying the appearance of macroscopic, often skeletonized, bilaterians during the Ediacaran–Cambrian diversification of animals requires carefully parsing the contributions of ecological opportunity, environmental potential and developmental capacity. The early evolution of animals involved the introduction of genomic, developmental, morphologic and behavioural novelties, identified as the individuation of new characters, which led to the construction of new ecological networks (innovation). Here I employ a recently introduced conceptual framework for novelty and i
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24

Soltis, Pamela S., Xiaoxian Liu, D. Blaine Marchant, Clayton J. Visger, and Douglas E. Soltis. "Polyploidy and novelty: Gottlieb's legacy." Philosophical Transactions of the Royal Society B: Biological Sciences 369, no. 1648 (2014): 20130351. http://dx.doi.org/10.1098/rstb.2013.0351.

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Nearly four decades ago, Roose & Gottlieb (Roose & Gottlieb 1976 Evolution 30 , 818–830. ( doi:10.2307/2407821 )) showed that the recently derived allotetraploids Tragopogon mirus and T. miscellus combined the allozyme profiles of their diploid parents ( T. dubius and T. porrifolius , and T. dubius and T. pratensis , respectively). This classic paper addressed the link between genotype and biochemical phenotype and documented enzyme additivity in allopolyploids. Perhaps more important than their model of additivity, however, was their demonstration of novelty at the biochemical level.
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25

Belshaw, R., O. G. Pybus, and A. Rambaut. "The evolution of genome compression and genomic novelty in RNA viruses." Genome Research 17, no. 10 (2007): 1496–504. http://dx.doi.org/10.1101/gr.6305707.

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26

Busch, A., S. Horn, A. Muhlhausen, K. Mummenhoff, and S. Zachgo. "Corolla Monosymmetry: Evolution of a Morphological Novelty in the Brassicaceae Family." Molecular Biology and Evolution 29, no. 4 (2011): 1241–54. http://dx.doi.org/10.1093/molbev/msr297.

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27

Tokita, Masayoshi, Takuya Kiyoshi, and Kyle N. Armstrong. "Evolution of craniofacial novelty in parrots through developmental modularity and heterochrony." Evolution & Development 9, no. 6 (2007): 590–601. http://dx.doi.org/10.1111/j.1525-142x.2007.00199.x.

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28

Parichy, David M. "Homology and the evolution of novelty duringDanio adult pigment pattern development." Journal of Experimental Zoology Part B: Molecular and Developmental Evolution 308B, no. 5 (2007): 578–90. http://dx.doi.org/10.1002/jez.b.21141.

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29

Dobrynin, Pavel, Ekaterina Matyunina, S. V. Malov, and A. P. Kozlov. "The Novelty of Human Cancer/Testis Antigen Encoding Genes in Evolution." International Journal of Genomics 2013 (2013): 1–7. http://dx.doi.org/10.1155/2013/105108.

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Abstract (sommario):
In order to be inherited in progeny generations, novel genes should originate in germ cells. Here, we suggest that the testes may play a special “catalyst” role in the birth and evolution of new genes. Cancer/testis antigen encoding genes (CT genes) are predominantly expressed both in testes and in a variety of tumors. By the criteria of evolutionary novelty, the CT genes are, indeed, novel genes. We performed homology searches for sequences similar to human CT in various animals and established that most of the CT genes are either found in humans only or are relatively recent in their origin.
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30

Dawson, Scott C., and Alexander R. Paredez. "Alternative cytoskeletal landscapes: cytoskeletal novelty and evolution in basal excavate protists." Current Opinion in Cell Biology 25, no. 1 (2013): 134–41. http://dx.doi.org/10.1016/j.ceb.2012.11.005.

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31

Yu, Yi, Yimei Hu, Han Qiao, and Shouyang Wang. "Co-evolution: A New Perspective for Business Model Innovation." Journal of Systems Science and Information 6, no. 5 (2018): 385–98. http://dx.doi.org/10.21078/jssi-2018-385-14.

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Abstract This paper combines the perspective of co-evolution with studies in the area of business model, reveals the phenomenon of business model co-evolution and explores the business model coevolution mechanism between firms through a case study. Findings and what other companies can learn from this study are as follows. Firstly, companies, be it leaders or not, can act as enablers for other party’s business model innovation. Secondly, companies can enable each other’s business model innovation by taking the perspective of business model co-evolution; Thirdly, the interdependence of the busi
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32

Dudney, Joan, Richard J. Hobbs, Robert Heilmayr, John J. Battles, and Katharine N. Suding. "Navigating Novelty and Risk in Resilience Management." Trends in Ecology & Evolution 33, no. 11 (2018): 863–73. http://dx.doi.org/10.1016/j.tree.2018.08.012.

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33

Gomes, Jorge, Paulo Urbano, and Anders Lyhne Christensen. "PMCNS." International Journal of Natural Computing Research 4, no. 2 (2014): 1–19. http://dx.doi.org/10.4018/ijncr.2014040101.

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Abstract (sommario):
Novelty search is an evolutionary approach in which the population is driven towards behavioural innovation instead of towards a fixed objective. The use of behavioural novelty to score candidate solutions precludes convergence to local optima. However, in novelty search, significant effort may be spent on exploration of novel, but unfit behaviours. We propose progressive minimal criteria novelty search (PMCNS) to overcome this issue. In PMCNS, novelty search can freely explore the behaviour space as long as the solutions meet a progressively stricter fitness criterion. We evaluate the perform
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34

Kanazawa, Satoshi. "Temperature and evolutionary novelty as forces behind the evolution of general intelligence." Intelligence 36, no. 2 (2008): 99–108. http://dx.doi.org/10.1016/j.intell.2007.04.001.

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35

Kapheim, Karen M. "Genomic sources of phenotypic novelty in the evolution of eusociality in insects." Current Opinion in Insect Science 13 (February 2016): 24–32. http://dx.doi.org/10.1016/j.cois.2015.10.009.

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36

Christensen-Dalsgaard, Jakob, and Catherine E. Carr. "Evolution of a sensory novelty: Tympanic ears and the associated neural processing." Brain Research Bulletin 75, no. 2-4 (2008): 365–70. http://dx.doi.org/10.1016/j.brainresbull.2007.10.044.

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37

Larson, Brendon M. H., and Christoph Kueffer. "Managing invasive species amidst high uncertainty and novelty." Trends in Ecology & Evolution 28, no. 5 (2013): 255–56. http://dx.doi.org/10.1016/j.tree.2013.01.013.

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38

Robertson, Bruce A., Jennifer S. Rehage, and Andrew Sih. "Ecological novelty and the emergence of evolutionary traps." Trends in Ecology & Evolution 28, no. 9 (2013): 552–60. http://dx.doi.org/10.1016/j.tree.2013.04.004.

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39

Stead, N. "SENSING NOVELTY IN HONEY BEES." Journal of Experimental Biology 216, no. 11 (2013): i—ii. http://dx.doi.org/10.1242/jeb.088229.

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40

Morris, Jake, Joseph J. Hanly, Simon H. Martin, et al. "Deep Convergence, Shared Ancestry, and Evolutionary Novelty in the Genetic Architecture of Heliconius Mimicry." Genetics 216, no. 3 (2020): 765–80. http://dx.doi.org/10.1534/genetics.120.303611.

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Convergent evolution can occur through different genetic mechanisms in different species. It is now clear that convergence at the genetic level is also widespread, and can be caused by either (i) parallel genetic evolution, where independently evolved convergent mutations arise in different populations or species, or (ii) collateral evolution in which shared ancestry results from either ancestral polymorphism or introgression among taxa. The adaptive radiation of Heliconius butterflies shows color pattern variation within species, as well as mimetic convergence between species. Using compariso
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41

Shubin, Neil H., and Charles R. Marshall. "Fossils, genes, and the origin of novelty." Paleobiology 26, S4 (2000): 324–40. http://dx.doi.org/10.1017/s0094837300026993.

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The origin of evolutionary novelty involves changes across the biological hierarchy: from genes and cells to whole organisms and ecosystems. Understanding the mechanisms behind the establishment of new designs involves integrating scientific disciplines that use different data and, often, different means of testing hypotheses. Discoveries from both paleontology and developmental genetics have shed new light on the origin of morphological novelties. The genes that play a major role in establishing the primary axes of the body and appendages, and that regulate the expression of the genes that ar
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42

Spain, Anne M., Lee R. Krumholz, and Mostafa S. Elshahed. "Abundance, composition, diversity and novelty of soil Proteobacteria." ISME Journal 3, no. 8 (2009): 992–1000. http://dx.doi.org/10.1038/ismej.2009.43.

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43

Selz, O. M., and O. Seehausen. "Interspecific hybridization can generate functional novelty in cichlid fish." Proceedings of the Royal Society B: Biological Sciences 286, no. 1913 (2019): 20191621. http://dx.doi.org/10.1098/rspb.2019.1621.

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The role of interspecific hybridization in evolution is still being debated. Interspecific hybridization has been suggested to facilitate the evolution of ecological novelty, and hence the invasion of new niches and adaptive radiation when ecological opportunity is present beyond the parental species niches. On the other hand, hybrids between two ecologically divergent species may perform less well than parental species in their respective niches because hybrids would be intermediate in performance in both niches. The evolutionary consequences of hybridization may hence be context-dependent, d
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44

Robalino, Nikolaus, and Arthur Robson. "The Evolution of Strategic Sophistication." American Economic Review 106, no. 4 (2016): 1046–72. http://dx.doi.org/10.1257/aer.20140105.

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This paper investigates the evolutionary foundation for our ability to attribute preferences to others, an ability that is central to conventional game theory. We argue here that learning others' preferences allows individuals to efficiently modify their behavior in strategic environments with a persistent element of novelty. Agents with the ability to learn have a sharp, unambiguous advantage over those who are less sophisticated because the former agents extrapolate to novel circumstances information about opponents' preferences that was learned previously. This advantage holds even with a s
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45

Geem, Zong Woo. "Research Commentary." International Journal of Applied Metaheuristic Computing 1, no. 4 (2010): 75–79. http://dx.doi.org/10.4018/jamc.2010100105.

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Recently a paper was published which claims “harmony search is equivalent to evolution strategies and because the latter is not popular currently, the former has no future. Also, research community was misguided by the former’s disguised novelty.” This paper is written to rebut the original paper’s claims by saying 1) harmony search is different from evolution strategies because each has its own uniqueness, 2) performance, rather than novelty, is an algorithm’s survival factor, and 3) the original paper was biased to mislead into a predefined conclusion.” Also, the shortcomings of current revi
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46

Möller, M., and Q. C. B. Cronk. "EVOLUTION OF MORPHOLOGICAL NOVELTY: A PHYLOGENETIC ANALYSIS OF GROWTH PATTERNS IN STREPTOCARPUS (GESNERIACEAE)." Evolution 55, no. 5 (2001): 918. http://dx.doi.org/10.1554/0014-3820(2001)055[0918:eomnap]2.0.co;2.

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47

Clausen, Tommy. "The liability of novelty: Its implications for survival and evolution of new firms." Academy of Management Proceedings 2018, no. 1 (2018): 17349. http://dx.doi.org/10.5465/ambpp.2018.17349abstract.

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48

Möller, M., and Q. C. B. Cronk. "EVOLUTION OF MORPHOLOGICAL NOVELTY: A PHYLOGENETIC ANALYSIS OF GROWTH PATTERNS IN STREPTOCARPUS (GESNERIACEAE)." Evolution 55, no. 5 (2007): 918–29. http://dx.doi.org/10.1111/j.0014-3820.2001.tb00609.x.

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49

Babonis, L. S., and M. Q. Martindale. "Old Cell, New Trick? Cnidocytes as a Model for the Evolution of Novelty." Integrative and Comparative Biology 54, no. 4 (2014): 714–22. http://dx.doi.org/10.1093/icb/icu027.

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50

Allf, Bradley C., Paul A. P. Durst, and David W. Pfennig. "Behavioral Plasticity and the Origins of Novelty: The Evolution of the Rattlesnake Rattle." American Naturalist 188, no. 4 (2016): 475–83. http://dx.doi.org/10.1086/688017.

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