The human task-evoked pupillary response provides a sensitive physiological index of the intensity and online resource demands of numerous cognitive processes (e.g., memory retrieval, problem solving, or target detection). Cognitive pupillometry is a wellestablished technique that relies upon precise measurement of these subtle response functions. Baseline variability of pupil diameter is a complex artifact that typically necessitates mathematical correction. A methodological paradox within pupillometry is that linear and nonlinear forms of baseline scaling both remain accepted baseline correction techniques, despite yielding highly disparate results. The task-evoked pupillary response (TEPR) could potentially scale nonlinearly, similar to autonomic functions such as heart rate, in which the amplitude of an evoked response diminishes as the baseline rises. Alternatively, the TEPR could scale similarly to the cortical hemodynamic response, as a linear function that is independent of its baseline. However, the TEPR cannot scale both linearly and nonlinearly. Our aim was to adjudicate between linear and nonlinear scaling of human TEPR. We manipulated baseline pupil size by modulating the illuminance in the testing room as participants heard abrupt pure-tone transitions (Exp. 1) or visually monitored word lists (Exp. 2). Phasic pupillary responses scaled according to a linear function across all lighting (dark, mid, bright) and task (tones, words) conditions, demonstrating that the TEPR is independent of its baseline amplitude. We discuss methodological implications and identify a need to reevaluate past pupillometry studies.

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A series of cyclic 2,6-bis-(1,2,3-triazolyl)-pyridine anion receptors with thiourea functionalities were synthesized by click reaction of 2,6-diazidopyridine with protected propargylamine followed by condensation of a bisthiocyanate derivative with a series of diamines. Their chloride binding affinities as well as their transport properties in POPC bilayers were examined. These receptors were found to function as anion carriers, which can mediate both Cl(-)/NO3(-) antiport and H(+)/Cl(-) symport, and the transport activity of these hosts were dominated by their lipophilicity.

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Taboo words represent a potent subset of natural language. It has been hypothesized that "tabooness" reflects an emergent property of negative valence and high physiological arousal of word referents. Many taboo words (e.g., dick, shit) are indeed consistent with this claim. Nevertheless, American English is also rife with negatively valenced, highly arousing words the usage of which is not socially condemned (e.g., cancer, abortion, welfare). We evaluated prediction of tabooness of single words and novel taboo compound words from a combination of phonological, lexical, and semantic variables (e.g., semantic category, word length). For single words, physiological arousal and emotional valence strongly predicted tabooness with additional moderating contributions from form (phonology) and meaning (semantic category). In Experiment 2, raters judged plausibility for combinations of common nouns with taboo words to form novel taboo compounds (e.g., shitgibbon). A mixture of formal (e.g., ratio of stop consonants, length) and semantic variables (e.g., ± receptacle, ± profession) predicted the quality of novel taboo compounding. Together, these studies provide complementary evidence for interactions between word form and meaning and an algorithmic prediction of tabooness in American English. We discuss applications for models of taboo word representation.