| Literature DB >> 31849777 |
Kyohei Tanaka1, Isso Nakamura2, Shinri Ohta3, Naoki Fukui4, Mihoko Zushi5, Hiroki Narita6, Kuniyoshi L Sakai1.
Abstract
Ever since the inception of generative linguistics, various dependency patterns have been widely discussed in the literature, particularly as they pertain to the hierarchy based on "weak generation" - the so-called Chomsky Hierarchy. However, humans can make any possible dependency patterns by using artificial means on a sequence of symbols (e.g., computer programing). The differences between sentences in human language and general symbol sequences have been routinely observed, but the question as to why such differences exist has barely been raised. Here, we address this problem and propose a theoretical explanation in terms of a new concept of "Merge-generability," that is, whether the structural basis for a given dependency is provided by the fundamental operation Merge. In our functional magnetic resonance imaging (fMRI) study, we tested the judgments of noun phrase (NP)-predicate (Pred) pairings in sentences of Japanese, an SOV language that allows natural, unbounded nesting configurations. We further introduced two pseudo-adverbs, which artificially force dependencies that do not conform to structures generated by Merge, i.e., non-Merge-generable; these adverbs enable us to manipulate Merge-generability (Natural or Artificial). By employing this novel paradigm, we obtained the following results. Firstly, the behavioral data clearly showed that an NP-Pred matching task became more demanding under the Artificial conditions than under the Natural conditions, reflecting cognitive loads that could be covaried with the increased number of words. Secondly, localized activation in the left frontal cortex, as well as in the left middle temporal gyrus and angular gyrus, was observed for the [Natural - Artificial] contrast, indicating specialization of these left regions in syntactic processing. Any activation due to task difficulty was completely excluded from activations in these regions, because the Natural conditions were always easier than the Artificial ones. And finally, the [Artificial - Natural] contrast resulted in the dorsal portion of the left frontal cortex, together with wide-spread regions required for general cognitive demands. These results indicate that Merge-generable sentences are processed in these specific regions in contrast to non-Merge-generable sentences, demonstrating that Merge is indeed a fundamental operation, which comes into play especially under the Natural conditions.Entities:
Keywords: Chomsky Hierarchy; Merge; Merge-generability; fMRI; inferior frontal gyrus; lateral premotor cortex; syntax
Year: 2019 PMID: 31849777 PMCID: PMC6895067 DOI: 10.3389/fpsyg.2019.02673
Source DB: PubMed Journal: Front Psychol ISSN: 1664-1078
FIGURE 1Basic types of Natural and Artificial sentences. We tested six sentence types each under Natural or Artificial conditions. Below each example in Japanese, phrases in Romaji and word-by-word translations in English are shown (NOM = a nominative case marker). Each type was presented as three visual stimuli in the order of noun phrases (NPs), an adverb, and predicates (Preds). The same subscript letters stand for structurally bound correspondences between an NP and a Pred in the sentence (S): e.g., NP and Pred indicate that these two elements are paired (Predit denotes the predicate of an indefinite subject “it”). Curved arrows also denote such NP-Pred pairings based on sentence structures. Each of tree structures represents unique structures for NPs and Preds. (A) There were six types of Natural sentences with four words. Left: three types of sentences with sorezore: e.g., “Akiko and [her] friend are running and sitting, respectively” (s4-1), “As for Taro, [his] limbs are thick and warm, respectively” (s4-2), and “We meet with Taro and talk [with him], respectively” (s4-3). Right: three types of sentences with tokidoki: e.g., “Kenta says that Hanako sometimes ran” (t4-1), “Akiko and [her] teacher say that it was sometimes bright” (t4-2), and “Taro says with Kenta that it was sometimes bright” (t4-3). (B) There were six types of Artificial sentences with four words, but only two of these are shown here. For the description of other four sentence types (k4-2, k4-3, h4-2, and h4-3), see the “Stimuli” section. Left: artificial cross-serial dependencies (pairing relations between NPs and Preds). Right: artificial nested dependencies. In these examples, pseudowords (“koregore” and “hokiboki”) artificially forced dependencies without conforming to Merge-generable structures.
FIGURE 2Behavioral data. (A) Accuracy for an NP-Pred matching task. Filled and open bars represent Natural and Artificial conditions, respectively, each with either 4W (two NPs and two predicates) or 6W (three NPs and three predicates) conditions. Error bars denote the standard error of the mean (SEM) for the participants. ∗Corrected p < 0.01. (B) Reaction times (RTs) from the onset of a question-set for judgment. Only correct trials were included for RTs.
FIGURE 3Modulation of the cortical activation by Natural and Artificial conditions. Regions identified by (A) Natural (4W), (B) Artificial (4W), (C) [Natural (4W and 6W) – Artificial (4W and 6W)], and (D) [Artificial (4W and 6W) – Natural (4W and 6W)]. Exclusive masks of [– Artificial (i.e., negative activation)] and [– Natural] (uncorrected p < 0.001) were applied to the comparisons of C and D, respectively. Activations were projected onto the left (L) and right lateral surfaces, and medial section (x = –9) of a standard brain (FDR-corrected p < 0.05). Each yellow dot indicates the local maxima of activated regions. See Table 1 for the stereotactic coordinates of activation foci.
Regions with enhanced activations under the Natural or Artificial condition.
| F3op | 44 | L | −60 | 11 | 8 | 4.9 | 653 |
| F3op/F3t | 44/45 | L | −54 | 14 | 5 | 4.8 | ∗ |
| F3t/F3O | 45/47 | L | −42 | 8 | −1 | 4.7 | ∗ |
| MTG | 21 | L | −66 | −34 | 2 | 4.6 | ∗ |
| AG | 39 | L | −51 | −52 | 26 | 5.8 | ∗ |
| LPMC | 6/8 | L | −33 | −7 | 47 | 4.9 | 785 |
| R | 21 | −7 | 53 | 4.6 | ∗ | ||
| pre-SMA/ACC | 6/8/32 | M | −9 | 11 | 47 | 5.9 | ∗ |
| M | 12 | 14 | 41 | 6.1 | ∗ | ||
| M | 12 | 5 | 59 | 4.4 | ∗ | ||
| LPMC | 6/8 | L | −54 | 8 | 35 | 4.3 | 165 |
| F3op | 44 | L | −45 | 8 | 23 | 5.7 | ∗ |
| L | −33 | 14 | 8 | 3.9 | ∗ | ||
| IPL | 7/40 | L | −27 | −55 | 50 | 4.6 | 176 |
| L | −18 | −67 | 47 | 4.1 | ∗ | ||
| SMG | 40 | L | −36 | −40 | 41 | 4.1 | ∗ |
| IPL | 7/40 | R | 27 | −52 | 44 | 7.2 | 274 |
| SOG | 7/19 | L | −27 | −73 | 26 | 5.3 | 592 |
| MOG | 18/19 | L | −27 | −82 | 14 | 4.9 | ∗ |
| IOG | 18/19 | L | −39 | −79 | −13 | 7.2 | ∗ |
| FG | 19 | L | −42 | −70 | −16 | 6.8 | ∗ |
| MOG | 18/19 | R | 30 | −85 | 14 | 4.9 | 417 |
| FG | 19 | R | 30 | −85 | −4 | Inf | ∗ |
| R | 39 | −67 | −10 | 6.2 | ∗ |