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  • Article
    Berent I, Dupuis A, Brentari D.
    PLoS One. 2013;8(4):e60617.
    All spoken languages encode syllables and constrain their internal structure. But whether these restrictions concern the design of the language system, broadly, or speech, specifically, remains unknown. To address this question, here, we gauge the structure of signed syllables in American Sign Language (ASL). Like spoken languages, signed syllables must exhibit a single sonority/energy peak (i.e., movement). Four experiments examine whether this restriction is enforced by signers and nonsigners. We first show that Deaf ASL signers selectively apply sonority restrictions to syllables (but not morphemes) in novel ASL signs. We next examine whether this principle might further shape the representation of signed syllables by nonsigners. Absent any experience with ASL, nonsigners used movement to define syllable-like units. Moreover, the restriction on syllable structure constrained the capacity of nonsigners to learn from experience. Given brief practice that implicitly paired syllables with sonority peaks (i.e., movement)--a natural phonological constraint attested in every human language--nonsigners rapidly learned to selectively rely on movement to define syllables and they also learned to partly ignore it in the identification of morpheme-like units. Remarkably, nonsigners failed to learn an unnatural rule that defines syllables by handshape, suggesting they were unable to ignore movement in identifying syllables. These findings indicate that signed and spoken syllables are subject to a shared phonological restriction that constrains phonological learning in a new modality. These conclusions suggest the design of the phonological system is partly amodal.
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  • Article
    Yang B, Han F, Li Y, Bai Y, Xie Z, Yang J, Liu T.
    Environ Sci Pollut Res Int. 2023 May;30(21):60607-60617.
    We used magnesium slag (MS) as a calcium source for modifying coal gasification coarse slag (CGCS) in the presence of NaOH to prepare a novel phosphate adsorbent (MS-CGCS). Ca2SiO4 in MS reacts with NaOH during the high-temperature synthesis process, with sodium displacing a part of the calcium content in Ca2SiO4 and entering the mineral lattice to form Na2CaSiO4. Hydroxide ions reacted with calcium in Ca2SiO4 to generate Ca(OH)2 and decomposed into CaO at a high temperature. The two newly formed species participated in the phosphate removal. The MS-CGCS adsorbent showed good phosphate removal performance over a wide pH range, with a maximum phosphate adsorption capacity of 50.14 mg/g, which was significantly higher than that of other reported adsorbents. The Langmuir and pseudo-second-order models described the adsorption process well, indicating it being a monolayer and chemisorption process. The main mechanisms of phosphate removal are as follows: electrostatic interaction between the positively charged MS-CGCS and negatively charged phosphate ions; the inner-sphere complexation of oxides of metal, such as magnesium, aluminum, and calcium, with phosphate ions; and the precipitation of phosphate ions with calcium ions. Precipitation contributes to ~ 32% of the phosphate removal. This study provides a new method for the development of phosphate adsorbents while recycling CGCS and MS.
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