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Built environment and behavior: spatial sampling using parcel data.

PURPOSE: The quality and economy of inferential research rely heavily on the sampling method. This paper addresses a methodological challenge in environment-behavior research: sampling respondents in relation to their built environmental characteristics. METHODS: A discussion of issues related to traditional neighborhood-based sampling serves to introduce a new spatial sampling strategy. Spatial sampling consists of defining conceptual population of interest, constructing spatial sample frame using parcel-level environmental data in GIS, examining the sample frame, determining the sampling design and size, and drawing the samples. An application of this method is illustrated using a recent study examining environmental correlates of walking and biking. RESULTS: Spatial sampling with parcel-level data ensures sufficient variations in and proper distributions of the environmental variables of interest, while controlling for the conditions of no interest. The use of the individual as unit of analysis offers an economic, generalizable, and easily interpretable approach to environment-behavior research, and discourages the potentially erroneous a priori definition of neighborhoods and aggregation problems. CONCLUSIONS: With its capacity to consider a broad range of detailed environmental variables, spatial sampling contributes to finding new or stronger environment-behavior associations and to the growing number of studies using the social ecologic model.

Bicycling↗

Concrete spatial language: see what I mean?

Conveying complex mental scenarios is at the heart of human language. Advances in cognitive linguistics suggest this is mediated by an ability to activate cognitive systems involved in non-linguistic processing of spatial information. In this fMRI-study, we compare sentences with a concrete spatial meaning to sentences with an abstract meaning. Using this contrast, we demonstrate that sentence meaning involving motion in a concrete topographical context, whether linked to animate or inanimate subjects nouns, yield more activation in a bilateral posterior network, including fusiform/parahippocampal, and retrosplenial regions, and the temporal-occipital-parietal junction. These areas have previously been shown to be involved in mental navigation and spatial memory tasks. Sentences with an abstract setting activate an extended largely left-lateralised network in the anterior temporal, and inferior and superior prefrontal cortices, previously found activated by comprehension of complex semantics such as narratives. These findings support a model of language, where the understanding of spatial semantic content emerges from the recruitment of brain regions involved in non-linguistic spatial processing.

Acoustic Stimulation↗

Cooperation between the hippocampus and the entorhinal cortex in spatial memory: a disconnection study.

It has been recently shown that lesions of parahippocampal areas including the entorhinal cortex do not disrupt place learning in the water maze, suggesting that the hippocampo-cortical circuitry is not important for spatial memory [Burwell RD, Saddoris MP, Bucci DJ, Wiig KA. Corticohippocampal contributions to spatial and contextual learning. J Neurosci 2004;24:3826-36]. The aim of the present study was to tax more directly the cooperation between the hippocampus and entorhinal cortex in two different spatial tasks, a place navigation task and a spontaneous object exploration task, using a disconnection procedure. Damaging the entorhinal-hippocampal system induced impairments in the two tasks but only in the spatial object exploration task rats with contralateral lesions displayed a greater deficit than rats with ipsilateral lesions. The results suggest that the cooperation between the hippocampus and the entorhinal cortex is modulated by the nature of the task and the cognitive processes involved in formation of spatial memory.

Animals↗

Influence of gender on working and spatial memory in the novel object recognition task in the rat.

Gender differences in many behavioural tasks have been observed in both humans and laboratory animals. The novel object recognition (NOR) task is increasingly used to investigate drug effects on working memory processes, although, the influence of sexually dimorphic behaviours have not yet been evaluated. In addition, the role of natural fluctuations in the sex steroids during the oestrous cycle has received little attention during object recognition tasks. Therefore, the aim of the current study was to investigate the influence of gender and oestrous cycle phase on working and spatial memory using the NOR task. Animals were tested in the NOR task and the spatial NOR task. Male and female rats completed an acquisition trial followed by an inter-trial interval of a specified length, then a final retention trial. Vaginal cytology enabled the influence of oestrous cycle phase to be determined in both the NOR and spatial NOR, each animal was tested during one phase of their regular oestrous cycle only. It was found that female rats performed significantly better than male rats in the standard NOR paradigm (p<0.05 compared to no significance (NS) at 3h, respectively), while male rats showed improved memory in the spatial NOR paradigm compared with female rats (p<0.05 compared to NS at 3h, respectively). There was no influence of phase of oestrous cycle on the NOR task, however, during the spatial NOR there was a significant improvement in ability when oestrogen and progesterone levels have been shown to be at their lowest (i.e. p<0.05 during oestrous compared to NS at other stages). In conclusion, it is clear that gonadal hormones can influence components of memory and gender is an important consideration in experimental design.

Analysis of Variance↗

Sleep deprivation impairs spatial memory and decreases extracellular signal-regulated kinase phosphorylation in the hippocampus.

Loss of sleep may result in memory impairment. However, little is known about the biochemical basis for memory deficits induced by sleep deprivation. Extracellular signal-regulated kinase (ERK) is involved in memory consolidation in different tasks. Phosphorylation of ERK is necessary for its activation and is an important step in mediating neuronal responses to synaptic activities. The aim of the present study was to determine the effects of total sleep deprivation (TSD) on memory and ERK phosphorylation in the brain. Rats were trained in Morris water maze to find a hidden platform (a spatial task) or a visible platform (a nonspatial task) after 6 h TSD or spontaneous sleep. TSD had no effect on spatial learning, but significantly impaired spatial memory tested 24 h after training. Nonspatial learning and memory were not impaired by TSD. Phospho-ERK levels in the hippocampus were significantly reduced after 6 h TSD compared to the controls and returned to the control levels after 2 h recovery sleep. Total ERK1 and ERK2 were slightly increased after 6 h TSD and returned to the control levels after 2 h recovery sleep. These alterations were not observed in the cortex after TSD. Protein phosphotase-1 and mitogen-activated protein kinase phosphatase-2, which dephosphorylates phospho-ERK, were also measured, but they were not altered by TSD. The impairments of both spatial memory and ERK phosphorylation indicate that the hippocampus is vulnerable to sleep loss. These results are consistent with the idea that decreased ERK activation in the hippocampus is involved in sleep deprivation-induced spatial memory impairment.

Animals↗

Improved selective and divided spatial attention in early blind subjects.

Spatial attention paradigms using auditory or tactile stimulation were used to explore neural and behavioral reorganization in early blind subjects. Although it is commonly assumed that blind subjects outperform sighted subjects in such tasks, the empirical data to confirm this remain controversial. Moreover, previous studies have often confounded factors of sensory acuity with those of attention. In the present work, we compared the performance of individually matched early blind and sighted subjects during auditory and tactile tasks. These consisted of sensory acuity tests, simple reaction time task as well as selective and divided spatial attention tasks. Based on sensory measurements, we made sure that the reliability and salience of auditory and tactile information were identical between the two populations to estimate attentional performance independently of sensory influence. Results showed no difference between groups in either sensory sensitivity or simple reaction time task for both modalities. However, blind subjects displayed shorter reaction times than sighted subjects in both tactile and auditory selective spatial attention tasks and also in bimodal divided spatial attention tasks. The present study thus demonstrates an enhanced attentional performance in early blind subjects which is independent of sensory influence. These supra-normal abilities could be related to quantitative and qualitative changes in the way early visually deprived subjects process non-visual spatial information.

Acoustic Stimulation↗

Effects of spatial distribution of attention during inhibition of return (IOR) on flanker interference in hearing and congenitally deaf people.

This study explored the interaction between the spatial distribution of attention during inhibition of return (IOR) and different levels of flanker interference in congenitally deaf subjects as compared with hearing subjects. Color (Experiment 1) and alphanumeric (Experiment 2) flanker interference effects were differentiated into the pre-response and the response levels. The spatial distribution of attention was manipulated through IOR. Subjects were asked to either make color or letter/digit discriminations to the central targets or detect the abrupt-onset peripheral targets. Deaf subjects were significantly faster than hearing subjects at detecting peripheral targets irrespective of the cue validity, while the two groups had comparable sizes of IOR. In the central discrimination tasks, deaf subjects showed significant response level, but not pre-response level, flanker effects irrespective of the type of stimuli and the spatial location of the flanker. For hearing subjects, however, spatial attention interacted with the pre-response and response flanker effects in different ways. While flankers at the cued location caused interference effects at the response level and facilitatory effects at the pre-response level, those at the uncued location caused different effects depending on the type of stimuli. Moreover, increasing the peripheral attention for hearing subjects, by increasing the proportion of peripheral detection trials, made hearing subjects behave like deaf subjects. These results demonstrate that deaf people possess enhanced peripheral attentional resources as compared with hearing people. The spatial distribution of attention modulates mainly the resolution of the pre-response flanker interference in hearing people, but affects neither the pre-response nor the response level interference in deaf people.

Acoustic Stimulation↗

Hallmarks of a common forebrain vertebrate plan: specialized pallial areas for spatial, temporal and emotional memory in actinopterygian fish.

In mammals and birds different pallial forebrain areas participate in separate memory systems. In particular, the hippocampal pallium is implicated in spatial memory and temporal attribute processing, whereas the amygdalar pallium is involved in emotional memory. Here we analyze the involvement of teleost fish lateral and medial pallia, proposed as homologous to the hippocampus and amygdala, respectively, in a variety of learning and memory tasks, such as spatial memory; reversal learning; delay or trace motor classical conditioning; heart rate, emotional classical conditioning; and two way active avoidance conditioning. Results show that the damage to the lateral pallium produces a profound deficit in spatial learning and memory in teleost fish. In addition, lateral pallium lesions produce a significant deficit in trace classical conditioning, whereas they have no significant effects on delay conditioning, or in heart rate conditioning. In contrast, medial pallium lesions disrupt emotional, heart rate conditioning and avoidance conditioning, but spare spatial memory and temporal stimulus processing. These data demonstrate a striking functional similarity between the medial and lateral pallia of teleost fish and the pallial amygdala and hippocampal pallium of land vertebrates, respectively. The reviewed evidence suggest that these two separate memory systems, the hippocampus-dependent spatial, relational or temporal memory system, and the amygdala based emotional memory system, could have appeared early during evolution, having conserved their functional identity through vertebrate phylogenesis.

Animals↗

Phytoplankton blooms and fish recruitment rate: effects of spatial distribution.

We consider the spatio-temporal dynamics of a spatially-structured generalization of the phytoplankton-zooplankton-fish larvae model system proposed earlier (Biktashev et al., 2003, J. Plankton Res. 5, 21-33; James et al., 2003, Ecol. Model. 160, 77-90). In contrast to Pitchford and Brindley (2001, Bull. Math. Biol. 63, 527-546), who were concerned with small scale patchiness (i.e., 1-10 m), on which the (stochastic) raptorial behaviour of individual larvae is important, we address here the much larger scale 'patchy' problems (i.e., 10-100 km), on which both larvae and plankton may be regarded as passive tracers of the fluid motion, dispersed and mixed by the turbulent diffusion processes. In particular, we study the dependence of the fish recruitment on carrying capacities of the plankton subsystem and on spatio-temporal evolution of that subsystem with respect to the larvae hatching site(s). It is shown that the main features found both in the nonstructured and age-structured spatially uniform models are observed in the spatially structured case, but that spatial effects can significantly modify the overall quantitative outcome. Spatial patterns in the metamorphosed fish distribution are a consequence of quasi-local interaction of larvae with plankton, in which the dispersion of larvae by large scale turbulent eddies plays little part due to the relatively short timescale of the larvae development. As a result, in a strong phyto/zooplankton subsystem, with fast reproduction rate and large carrying capacity of phytoplankton and high conversion ratio of zooplankton, recruitment success depends only on the localization and timing of the hatching with respect to the plankton patches. In a weak phyto/zooplankton system, with slow reproduction rate and small carrying capacity of phytoplankton and low conversion ratio of zooplankton, the larvae may significantly influence the evolution of the plankton patches, which may lead to nontrivial cooperative effects between different patches of larvae. However, in this case, recruitment is very low.

Animals↗

Effect of spatial attention on human sensorimotor integration studied by transcranial magnetic stimulation.

OBJECTIVE: Recent transcranial magnetic stimulation (TMS) studies showed that the sensory input can decrease the motor cortex excitability (afferent inhibition). To clarify the effect of attention on sensorimotor integration, we investigated the effect of spatial attention on afferent inhibition. METHODS: Right median nerve electrical stimulation followed, at variable delays (10-300 ms), by TMS over the left motor cortex was applied to 9 subjects, during 3 conditions; spatial attention to the right and left hand, and control (no attention) tasks. RESULTS: Inhibition of the motor evoked potential occurred at inter-stimulus interval of 20 and 100 ms, which was more was marked during spatial attention to the right than to the left hand. CONCLUSIONS: Enhancement of the afferent inhibition induced by spatial attention to the stimulated side is likely to reflect the interaction between attention and sensorimotor integration. SIGNIFICANCE: The spatial attention may modulate the sensorimotor integration studied by afferent inhibition of the MEP.

Adult↗

Evaluating the effects of spatial frequency on migraines by using pattern-reversal visual evoked potentials.

OBJECTIVE: To clarify the effects of contrast and spatial frequency in patients with migraine by means of pattern-reversal visual evoked potentials (PVEPs). METHODS: PVEPs were obtained from 14 patients who had migraine without aura (MO), 11 patients who had migraine with aura (MA), and 25 age-matched, healthy controls (CO). PVEPs were binocularly recorded with a reversal rate of 1Hz (2 reversal/s) at 3 spatial frequencies (0.5, 1.0 and 4.0 cpd) at high (98%), medium (83%) and low (29%) contrast. N75, P100 and N135 latency and the amplitudes of P50-N75, N75-P100 and P100-N135 were analyzed. RESULTS: Increased amplitude of PVEPs in patients with migraines were revealed at 3 different spatial frequencies in all components. The MO and the MA showed increased amplitudes mostly in high contrasts (98%). These findings were detected more at a high spatial frequency (4.0 cpd) than at a low spatial frequency (0.5 cpd). Increased amplitude with prolonged latency of N135 were found both in MO and MA at 4.0 cpd. CONCLUSIONS: We conclude that pattern stimuli of high contrasts may be particularly effective in uncovering abnormal cortical reactivity which may be modified in the primary and secondary visual cortex in the interictal state of migraine. SIGNIFICANCE: These findings indicate that there is abnormal visual cortex processing in patients with migraine.

Adult↗

Modelling of discrete spatial variation in epidemiology with SAS using GLIMMIX.

SAS provides a macro GLIMMIX, which can be used for modelling of discrete spatial variation in epidemiological studies, where data are aggregated into small areas such as municipalities or postcode sectors. The purpose of these models is primary to examine to what extent unmeasured spatially correlated variables can explain the outcome of interest. Some necessary additional code is proposed for this macro implementing some of the most used models for analysing and exploring spatial variation, in for example Poisson and logistic regression: Gaussian intrinsic conditional autoregression and spatial multiple memberships models originated from multilevel models. The code is illustrated by analysing the well-known Scottish lip cancer dataset with GLIMMIX and the results are compared with a Markov chain Monte Carlo approach. The code gives epidemiologists and bio-statisticians an immediate tool for analysing discrete spatial models in a familiar statistical software package.

Biometry↗

Hemispheric asymmetry for spatially filtered stimuli belonging to different semantic categories.

The hemispheric specialization for processing visual stimuli as a function of spatial-frequency content and semantic category was investigated. Spatially filtered pictures of animals and tools were displayed to both hemifields at nine levels of spatial-frequency filtering following a coarse-to-fine design. Results showed a differential hemispheric specialization in relation to the semantic category of stimuli. Animals might be identified at low spatial frequencies (coarse information) in a similar extent in both hemifield conditions, while a hemispheric dissociation was found for tools (the increasing of levels of high-spatial frequency information was especially needed when such stimuli were presented to the left visual field /right hemisphere (RH) relative to that for right visual field/left hemisphere presentations).

Adult↗

Spatial processing in human auditory cortex: the effects of 3D, ITD, and ILD stimulation techniques.

Here, the perception of auditory spatial information as indexed by behavioral measures is linked to brain dynamics as reflected by the N1m response recorded with whole-head magnetoencephalography (MEG). Broadband noise stimuli with realistic spatial cues corresponding to eight direction angles in the horizontal plane were constructed via custom-made, individualized binaural recordings (BAR) and generic head-related transfer functions (HRTF). For comparison purposes, stimuli with impoverished acoustical cues were created via interaural time and level differences (ITDs and ILDs) and their combinations. MEG recordings in ten subjects revealed that the amplitude and the latency of the N1m exhibits directional tuning to sound location, with the amplitude of the right-hemispheric N1m being particularly sensitive to the amount of spatial cues in the stimuli. The BAR, HRTF, and combined ITD + ILD stimuli resulted both in a larger dynamic range and in a more systematic distribution of the N1m amplitude across stimulus angle than did the ITD or ILD stimuli alone. Further, the right-hemispheric source loci of the N1m responses for the BAR and HRTF stimuli were anterior to those for the ITD and ILD stimuli. In behavioral tests, we measured the ability of the subjects to localize BAR and HRTF stimuli in terms of azimuthal error and front-back confusions. We found that behavioral performance correlated positively with the amplitude of the N1m. Thus, the activity taking place already in the auditory cortex predicts behavioral sound detection of spatial stimuli, and the amount of spatial cues embedded in the signal are reflected in the activity of this brain area.

Acoustic Stimulation↗

The role of spatial frequency information for ERP components sensitive to faces and emotional facial expression.

To investigate the impact of spatial frequency on emotional facial expression analysis, ERPs were recorded in response to low spatial frequency (LSF), high spatial frequency (HSF), and unfiltered broad spatial frequency (BSF) faces with fearful or neutral expressions, houses, and chairs. In line with previous findings, BSF fearful facial expressions elicited a greater frontal positivity than BSF neutral facial expressions, starting at about 150 ms after stimulus onset. In contrast, this emotional expression effect was absent for HSF and LSF faces. Given that some brain regions involved in emotion processing, such as amygdala and connected structures, are selectively tuned to LSF visual inputs, these data suggest that ERP effects of emotional facial expression do not directly reflect activity in these regions. It is argued that higher order neocortical brain systems are involved in the generation of emotion-specific waveform modulations. The face-sensitive N170 component was neither affected by emotional facial expression nor by spatial frequency information.

Adult↗

Have sex differences in spatial ability evolved from male competition for mating and female concern for survival?

Drawing on the theoretical and empirical foundations of two evolutionary models, we argue that, among humans and other mammals, a twofold selection process would parsimoniously account for sex-linked advantages in spatial contexts. In males, a superiority for both solving navigation-related spatial problems and understanding physical principles that apply to the behavior of projectiles could have been inherited from mating-oriented male competition involving extensive ranging and agonistic displays. In females, a form of superior spatial memory may have been shaped in relation to a costly reproduction system compelling them to safeguard their survival and that of their offspring by fostering low-risk strategies consisting of restricted navigation as well as concentration on nearby spatial cues. Based on the combined action of competition and survival pressures, we submit new predictions as to spatial sex differences in several species including humans.

Animals↗

Visually induced plasticity of auditory spatial perception in macaques.

When experiencing spatially disparate visual and auditory stimuli, a common percept is that the sound originates from the location of the visual stimulus, an illusion known as the ventriloquism effect. This illusion can persist for tens of minutes, a phenomenon termed the ventriloquism aftereffect. The underlying neuronal mechanisms of this rapidly induced plasticity remain unclear; indeed, it remains untested whether similar multimodal interactions occur in other species. We therefore tested whether macaque monkeys experience the ventriloquism aftereffect similar to the way humans do. The ability of two monkeys to determine which side of the midline a sound was presented from was tested before and after a period of 20-60 min in which the monkeys experienced either spatially identical or spatially disparate auditory and visual stimuli. In agreement with human studies, the monkeys did experience a shift in their auditory spatial perception in the direction of the spatially disparate visual stimulus, and the aftereffect did not transfer across sounds that differed in frequency by two octaves. These results show that macaque monkeys experience the ventriloquism aftereffect similar to the way humans do in all tested respects, indicating that these multimodal interactions are a basic phenomenon of the central nervous system.

Acoustic Stimulation↗

Chocolate cravings are susceptible to visuo-spatial interference.

The study investigated the specificity of visuo-spatial working memory-based techniques as a means to reduce chocolate cravings. Twenty-four self-identified chocolate cravers and 24 non-cravers formed and maintained images of chocolate-containing foods elicited by pictures, while performing a visuo-spatial task (loading the visuo-spatial sketch pad) or an auditory task (loading the phonological loop). Vividness and craving intensity were rated for each image. Concurrent visuo-spatial processing was found to render chocolate images significantly less vivid and cravings less intense compared to concurrent verbal processing, for both cravers and non-cravers. Chocolate cravers did, however, report higher levels of chocolate craving and intake than non-cravers. It was concluded that visuo-spatial tasks provide an effective craving reduction mechanism for the management of chocolate cravings. Such techniques may be particularly useful in populations for whom eating problems are triggered by chocolate craving.

Adolescent↗