Publications

Abstract

We are often in a bilingual situation (e.g., overhearing a conversation in the train). We investigated whether first (L1) and second language (L2) phonologies are automatically activated. A masked priming paradigm was used, with Russian words as targets and either Russian or English words as primes. Event-related potentials (ERPs) were recorded while Russian (L1) – English (L2) bilinguals read aloud L1 target words (e.g. РЕЙС /reis/ ‘fl ight’) primed with either L1 (e.g. РАНА /rana/ ‘wound’) or L2 words (e.g. PACK). Target words were read faster when they were preceded by phonologically related L1 primes but not by orthographically related L2 primes. ERPs showed orthographic priming in the 125-200 ms time window. Thus, both L1 and L2 phonologies are simultaneously activated during L1 reading. The results provide support for non-selective models of bilingual reading, which assume automatic activation of the non-target language phonology even when it is not required by the task.

Abstract

In her path-breaking 1986 paper, Johanna Nichols proposed a typological contrast between head-marking and dependent-marking languages. Nichols argues that even though the syntactic relations between the head and its dependents are the same in both types of language, the syntactic “bond” between them is not the same; in dependent-marking languages it is one of government, whereas in head-marking languages it is one of apposition. This distinction raises an important question for linguistic theory: How can this contrast – government versus apposition – which can show up in all of the major phrasal types in a language, be captured? The purpose of this paper is to explore the various approaches that have been taken in an attempt to capture the difference between head-marked and dependent-marked syntax in different linguistic theories. The basic problem that head-marking languages pose for syntactic theory will be presented, and then generative approaches will be discussed. The analysis of head-marked structure in Role and Reference Grammar will be presented

Abstract

Disorders of speech and language are highly heritable, providing strong
support for a genetic basis. However, the underlying genetic architecture is complex,
involving multiple risk factors. This chapter begins by discussing genetic loci associated
with common multifactorial language-related impairments and goes on to
detail the only gene (known as FOXP2) to be directly implicated in a rare monogenic
speech and language disorder. Although FOXP2 was initially uncovered in
humans, model systems have been invaluable in progressing our understanding of
the function of this gene and its associated pathways in language-related areas of the
brain. Research in species from mouse to songbird has revealed effects of this gene
on relevant behaviours including acquisition of motor skills and learned vocalisations
and demonstrated a role for Foxp2 in neuronal connectivity and signalling,
particularly in the striatum. Animal models have also facilitated the identification of
wider neurogenetic networks thought to be involved in language development and
disorder and allowed the investigation of new candidate genes for disorders involving
language, such as CNTNAP2 and FOXP1. Ongoing work in animal models promises
to yield new insights into the genetic and neural mechanisms underlying human
speech and language

Abstract

The ISOcat Data Category Registry provides a community computing environment for creating, storing, retrieving, harmonizing and standardizing data category specifications (DCs), used to register linguistic terms used in various fields. This chapter recounts the history of DC documentation in TC 37, beginning from paper-based lists created for lexicographers and terminologists and progressing to the development of a web-based resource for a much broader range of users. While describing the considerable strides that have been made to collect a very large comprehensive collection of DCs, it also outlines difficulties that have arisen in developing a fully operative web-based computing environment for achieving consensus on data category names, definitions, and selections and describes efforts to overcome some of the present shortcomings and to establish positive working procedures designed to engage a wide range of people involved in the creation of language resources.

Abstract

This paper reports on an exploration of the ways in which multiple entities are expressed in Turkish Sign Language (TİD). The (descriptive and quantitative) analyses provided are based on a corpus of both spontaneous data and specifically elicited data, in order to provide as comprehensive an account as possible. We have found several devices in TİD for expression of multiple entities, in particular localization, spatial plural predicate inflection, and a specific form used to express multiple entities that are side by side in the same configuration (not reported for any other sign language to date), as well as numerals and quantifiers. In contrast to some other signed languages, TİD does not appear to have a productive system of plural reduplication. We argue that none of the devices encountered in the TİD data is a genuine plural marking device and that the plural interpretation of multiple entity localizations and plural predicate inflections is a by-product of the use of space to indicate the existence or the involvement in an event of multiple entities.