Listener evaluation of sociophonetic variability : probing constraints and capabilities

This paper reports the results of an experimental study designed to investigate how listeners learn to create new associations between phonetic properties of the speech signal and external social referents. Very little is known of how this learning takes place in children, and it is a particularly challenging area to study given the difficulty in controlling some of the variables which are likely to be important factors in children's learning of the productive and interpretative dimensions of social-indexical phonetic variation. Thus, in this study, we focus on adult listeners in order to develop a sense of how adults might approach this learning task, and also to test out a method for probing this form of learning in a controlled fashion. 49 participants were trained on new patterns of social-indexical variability and, in a subsequent test phase, we assessed the extent to which this training led the listeners to acquire new associations between specific realizational variants and the social categories with which they have been associated in the training material. Results are reported from four experimental conditions which provided listeners with a range of different learning tasks. Our findings suggest that learning of novel sociophonetic associations can be achieved as the result of a relatively short amount of exposure to training material incorporating the new association, but that the success with which learning takes place is dependent on a number of factors such as the nature of the criterial variable and individual learner variation.Full Tex

An Information Theoretic perspective on perceptual structure: cross-accent vowel perception

Analytical tools from Information Theory were used to quantify behaviour in cross-accent vowel perception by Australian, London, New Zealand, Yorkshire and Newcastle UK listeners. Results show that Australian listeners impose expected patterns of perceptual similarity from their own accent experience on unfamiliar accents, regardless of the actual phonetic distance between accents

Three steps forward for predictability : Consideration of methodological robustness, indexical and prosodic factors, and replication in the laboratory

There is now abundant evidence that phonetic forms are shaped by probabilistic effects reflecting predictability or informativity. We outline a number of challenges for such work, where theoretical claims are often based on small differences in acoustic measurements, or interpretations of small statistical effect sizes. We outline caveats about the methods and assumptions encountered in many studies of predictability effects, particularly regarding corpus-based approaches. We consider the wide range of factors that influence patterns of variability in phonetic forms, taking a broad perspective on what is meant by “the message” in order to show that predictability effects need to be considered alongside many others, including indexical and prosodic factors. We suggest a number of ways forward to extend our understanding of the form-predictability relationship.Full Tex

Resilience of English vowel perception across regional accent variation

In two categorization experiments using phonotactically legal nonce words, we tested Australian English listeners’ perception of all vowels in their own accent as well as in four less familiar regional varieties of English which differ in how their vowel realizations diverge from Australian English: London, Yorkshire, Newcastle (UK), and New Zealand. Results of Experiment 1 indicated that amongst the vowel differences described in sociophonetic studies and attested in our stimulus materials, only a small subset caused greater perceptual difficulty for Australian listeners than for the corresponding Australian English vowels. We discuss this perceptual tolerance for vowel variation in terms of how perceptual assimilation of phonetic details into abstract vowel categories may contribute to recognizing words across variable pronunciations. Experiment 2 determined whether short-term multi-talker exposure would facilitate accent adaptation, particularly for those vowels that proved more difficult to categorize in Experiment 1. For each accent separately, participants listened to a pre-test passage in the nonce word accent but told by novel talkers before completing the same task as in Experiment 1. In contrast to previous studies showing rapid adaptation to talker-specific variation, our listeners’ subsequent vowel assimilations were largely unaffected by exposure to other talkers’ accent-specific variation

Revealing perceptual structure through input variation: cross-accent categorization of vowels in five accents of English

This paper characterizes the perceptual structure of vowel systems in five regional accents of English, from Australia (A), New Zealand (Z), London (L), Yorkshire (Y), and Newcastle upon Tyne (N), on the basis of “whole system” vowel categorization experiments. We established patterns of within-accent vowel confusions, and then explored cross-accent perception, assessing how listeners from one accent background categorize vowels from another. Our experimental task required mapping continuous phonetic dimensions to perceptual categories in the absence of phonotactic and lexical cues to vowel identity and socio-indexical information about the talker. Our results show that, without these sources of information, there is uncertainty in vowel categorization, even for native accent vowels, and that this degree of uncertainty increases for unfamiliar accents. The patterns of cross-accent perception largely reflect the accent-specific perceptual structure of the listener, as opposed to adaptations to the stimulus accents. This finding contrasts with the type of active talker adaptation found with tasks offering lexical information about vowel identity and indexical information about the talker

Constructing social meaning in political discourse: Phonetic variation and verb processes in Ed Miliband's speeches

This article investigates how variation across different levels of linguistic structure indexes ideological alignments in political talk. We analyse two political speeches by Ed Miliband, the former leader of the UK Labour Party, with a focus on the use of /t/-glottalling and the types of verb processes that co-occur with the pronouns we and you. We find substantial differences in the production of /t/ between the two speeches in words such as Britain and government, which have been argued to take on particular salience in British political discourse. We contextualise these findings in terms of metalinguistic discourse surrounding Miliband's language use, as well as how he positions himself in relation to different audiences via verb process types. We show that phonetic variation, subject types, and verb processes work synergistically in allowing Miliband to establish a political persona that is sensitive to ideological differences between different audiences. (Social meaning, indexicality, political discourse, verb processes, phonetic variation, /t/-glottalling)*

Chromosomal radiosensitivity in head and neck cancer patients: evidence for genetic predisposition?

The association between chromosomal radiosensitivity and genetic predisposition to head and neck cancer was investigated in this study. In all, 101 head and neck cancer patients and 75 healthy control individuals were included in the study. The G2 assay was used to measure chromosomal radiosensitivity. The results demonstrated that head and neck cancer patients had a statistically higher number of radiation-induced chromatid breaks than controls, with mean values of 1.23 and 1.10 breaks per cell, respectively (P<0.001). Using the 90th percentile of the G2 scores of the healthy individuals as a cutoff value for chromosomal radiosensitivity, 26% of the cancer patients were radiosensitive compared with 9% of the healthy controls (P=0.008). The mean number of radiation-induced chromatid breaks and the proportion of radiosensitive individuals were highest for oral cavity cancer patients (1.26 breaks per cell, 38%) and pharynx cancer patients (1.27 breaks per cell, 35%). The difference between patients and controls was most pronounced in the lower age group (⩽50 years, 1.32 breaks per cell, 38%) and in the non- and light smoking patient group (⩽10 pack-years, 1.28 breaks per cell, 46%). In conclusion, enhanced chromosomal radiosensitivity is a marker of genetic predisposition to head and neck cancer, and the genetic contribution is highest for oral cavity and pharynx cancer patients and for early onset and non- and light smoking patients

Structured speaker variability in Japanese stops: relationships within versus across cues to stop voicing

A number of recent studies have observed that phonetic variability is constrained across speakers, where speakers exhibit limited variation in the signalling of phonological contrasts in spite of overall differences between speakers. This previous work focused predominantly on controlled laboratory speech and on contrasts in English and German, leaving unclear how such speaker variability is structured in spontaneous speech and in phonological contrasts that make substantial use of more than one acoustic cue. This study attempts to both address these empirical gaps and expand the empirical scope of research investigating structured variability by examining how speakers vary in the use of positive voice onset time and voicing during closure in marking the stop voicing contrast in Japanese spontaneous speech. Strong covarying relationships within each cue across speakers are observed, while between-cue relationships across speakers are much weaker, suggesting that structured variability is constrained by the language-specific phonetic implementation of linguistic contrasts

The impact of viral mutations on recognition by SARS-CoV-2 specific T cells.

We identify amino acid variants within dominant SARS-CoV-2 T cell epitopes by interrogating global sequence data. Several variants within nucleocapsid and ORF3a epitopes have arisen independently in multiple lineages and result in loss of recognition by epitope-specific T cells assessed by IFN-γ and cytotoxic killing assays. Complete loss of T cell responsiveness was seen due to Q213K in the A∗01:01-restricted CD8+ ORF3a epitope FTSDYYQLY207-215; due to P13L, P13S, and P13T in the B∗27:05-restricted CD8+ nucleocapsid epitope QRNAPRITF9-17; and due to T362I and P365S in the A∗03:01/A∗11:01-restricted CD8+ nucleocapsid epitope KTFPPTEPK361-369. CD8+ T cell lines unable to recognize variant epitopes have diverse T cell receptor repertoires. These data demonstrate the potential for T cell evasion and highlight the need for ongoing surveillance for variants capable of escaping T cell as well as humoral immunity.This work is supported by the UK Medical Research Council (MRC); Chinese Academy of Medical Sciences(CAMS) Innovation Fund for Medical Sciences (CIFMS), China; National Institute for Health Research (NIHR)Oxford Biomedical Research Centre, and UK Researchand Innovation (UKRI)/NIHR through the UK Coro-navirus Immunology Consortium (UK-CIC). Sequencing of SARS-CoV-2 samples and collation of data wasundertaken by the COG-UK CONSORTIUM. COG-UK is supported by funding from the Medical ResearchCouncil (MRC) part of UK Research & Innovation (UKRI),the National Institute of Health Research (NIHR),and Genome Research Limited, operating as the Wellcome Sanger Institute. T.I.d.S. is supported by a Well-come Trust Intermediate Clinical Fellowship (110058/Z/15/Z). L.T. is supported by the Wellcome Trust(grant number 205228/Z/16/Z) and by theUniversity of Liverpool Centre for Excellence in Infectious DiseaseResearch (CEIDR). S.D. is funded by an NIHR GlobalResearch Professorship (NIHR300791). L.T. and S.C.M.are also supported by the U.S. Food and Drug Administration Medical Countermeasures Initiative contract75F40120C00085 and the National Institute for Health Research Health Protection Research Unit (HPRU) inEmerging and Zoonotic Infections (NIHR200907) at University of Liverpool inpartnership with Public HealthEngland (PHE), in collaboration with Liverpool School of Tropical Medicine and the University of Oxford.L.T. is based at the University of Liverpool. M.D.P. is funded by the NIHR Sheffield Biomedical ResearchCentre (BRC – IS-BRC-1215-20017). ISARIC4C is supported by the MRC (grant no MC_PC_19059). J.C.K.is a Wellcome Investigator (WT204969/Z/16/Z) and supported by NIHR Oxford Biomedical Research Centreand CIFMS. The views expressed are those of the authors and not necessarily those of the NIHR or MRC