| Literature DB >> 23776488 |
Anita Eerland1, Jan A A Engelen, Rolf A Zwaan.
Abstract
Language can be viewed as a set of cues that modulate the comprehender's thought processes. It is a very subtle instrument. For example, the literature suggests that people perceive direct speech (e.g., Joanne said: 'I went out for dinner last night') as more vivid and perceptually engaging than indirect speech (e.g., Joanne said that she went out for dinner last night). But how is this alleged vividness evident in comprehenders' mental representations? We sought to address this question in a series of experiments. Our results do not support the idea that, compared to indirect speech, direct speech enhances the accessibility of information from the communicative or the referential situation during comprehension. Neither do our results support the idea that the hypothesized more vivid experience of direct speech is caused by a switch from the visual to the auditory modality. However, our results do show that direct speech leads to a stronger mental representation of the exact wording of a sentence than does indirect speech. These results show that language has a more subtle influence on memory representations than was previously suggested.Entities:
Mesh:
Year: 2013 PMID: 23776488 PMCID: PMC3680483 DOI: 10.1371/journal.pone.0065480
Source DB: PubMed Journal: PLoS One ISSN: 1932-6203 Impact factor: 3.240
Critical Dependent Measures from all Experiments.
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| Direct M (SD) | Indirect M (SD) |
| Effect size (Cohen’s |
| |
|
| ||||||
| Probe RT | 154 | 1260 (420) | 1225 (386) | .15 | .09 | 5.55 |
| Probe RT 1b | 184 | 1357 (526) | 1355 (495) | .93 | .004 | 17.02 |
| 1a and 1b combined | 338 | 12.79 | ||||
| Probe Accuracy 1a | 154 | .96 (.06) | .95 (.07) | .80 | .15 | 15.17 |
| Probe Accuracy 1b | 184 | .95 (.06) | .94 (.08) | .03 | .14 | 1.66 |
| 1a and 1b combined | 338 | .002 | ||||
|
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| Probe RT 2a | 168 | 1209 (467) | 1144 (446) | .001 | .14 | .03 |
| Probe RT 2b | 176 | 1210 (446) | 1168 (420) | .03 | .09 | 1.56 |
| 2a and 2b combined | 344 | .01 | ||||
| Probe Accuracy 2a | 168 | .93 (.10) | .94 (.08) | .1 | −.11 | 4.27 |
| Probe Accuracy 2b | 176 | .91 (.12) | .93 (.11) | .002 | −.17 | .16 |
| 2a and 2b combined | 344 | .06 | ||||
|
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| Reading times 3a | 172 | 2842 (986) | 2916 (983) | .069 | .08 | 3 |
| Reading times 3b | 174 | 3129 (1047) | 3096 (1082) | .401 | .03 | 12 |
| 3a and 3b combined | 346 | 14 | ||||
| Probe RT 3a | 172 | 1540 (602) | 1537 (622) | .922 | .00 | 16 |
| Probe RT 3b | 174 | 1613 (769) | 1557 (709) | .086 | .07 | 4 |
| 3a and 3b combined | 346 | 8 | ||||
| Probe Accuracy 3a | 172 | .79 (.18) | .85 (.15) | .000 | .36 | .00 |
| Probe Accuracy 3b | 174 | .82 (18) | .86 (.15) | .000 | .32 | .01 |
| 3a and 3b combined | 346 | .00 | ||||
|
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| Probe RT 4a | 140 | 2607 (870) | 2569 (890) | .28 | .04 | 8.56 |
| Probe RT 4b | 144 | 3060 (1042) | 2997 (1034) | .02 | .06 | 1.20 |
| 4a and 4b combined | 284 | 1.63 | ||||
| Probe Accuracy 4a | 140 | .95 (.07) | .94 (.07) | .54 | .14 | 12.40 |
| Probe Accuracy 4b | 144 | .92 (.13) | .93 (.10) | .20 | −.09 | 6.74 |
| 4a and 4b combined | 284 | 16.95 | ||||
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| 188 | 1.88 (1.37) | 1.55 (1.30) | .006 | .24 | .42 |
|
| 188 | 1.90 (1.27) | 1.57 (1.25) | .002 | .26 | .15 |
| 5a and 5b combined | 376 | .01 | ||||
| C | 188 | 0.27 (0.79) | 0.29 (0.64) | .96 | −0.03 | 17.25 |
| C 5b | 188 | −0.21 (0.67) | −0.19 (0.66) | .56 | −0.03 | 14.62 |
BF = Bayes factor; RT = response time in milliseconds; d’ = measure of sensitivity, C = measure of tendency to respond ‘yes’.