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Constraints on priming in spatial memory: naturally learned versus experimentally learned environments.

In four experiments, we explored constraints on priming in spatial memory. In Experiments 1 and 2, subjects who were familiar with the locations of buildings on the Vanderbilt campus participated in a recognition test. The subjects' task was to decide whether or not named buildings were on the campus. Foils in this recognition test were realistic but fictional names of buildings. In principle, the subjects could have performed this task without using spatial knowledge; in fact, they must not have used spatial knowledge, because there was no evidence of priming in recognition as a function of the spatial relations between buildings on the campus. This result differs from those obtained in earlier experiments that have examined memory of spatial layouts learned in laboratory settings. In Experiment 3, the fictional foils were replaced by names of buildings in an area of the campus separated geographically from the main campus. Evidently, this change induced subjects to retrieve spatial knowledge, because the spatial priming effect materialized. A fourth experiment replicated the above findings in a single experiment and demonstrated that spatial priming could be obtained when the configuration of buildings was learned experimentally. These results are explained by appealing to the "decontextualization" that takes place in memory over time.

Adult↗

The precision of velocity discrimination across spatial frequency.

The precision of velocity coding for moving stimuli of different spatial frequencies was assessed by measuring velocity discrimination thresholds for a 1-c/deg grating paired with a grating whose spatial frequency ranged from 0.25 to 4 c/deg and for grating pairs of the same spatial frequency (0.25, 1, and 4 c/deg). The gratings always moved upward, with velocities ranging from 0.5 to 16 deg/sec. Velocity discrimination was as precise for stimuli that varied in spatial frequency by +/- 2 octaves (0.25 vs. 1 c/deg and 4 vs. 1 c/deg) as for stimuli of the same spatial frequency, for specific ranges of velocity that depended on the spatial and, therefore, the temporal frequencies of the stimuli. Compared with a 1-c/deg grating, the perceived velocity of 4-c/deg gratings was about 1.3 times faster and that of 0.25-c/deg gratings was about 1.3 times slower. Although these perceived velocity biases imply variation of velocity-signal processing among spatial frequency channels, the discrimination results indicate that the motion-sensing system can compare signals across different spatial frequency channels to make fine velocity discrimination within appropriate temporal frequency limits.

Acceleration↗

[Distribution of spatial attention in position recognition].

Spatial limitation in visual information processing was examined with dot-in-matrix patterns by using a probe recognition procedure. The independent variables were the number (1-16 dots) and the position of target dots. Subjects were four undergraduate students. The data were analyzed and discussed from three points of view; span of attention, spatial limitation of recognition and visual attention. The following became clear: First, the span of position recognition was 4.8. Second, "spatial span of attention" was defined as the range of dot positions at which subjects can perceive target dots with 75% or more accuracy. It extended around the fixation point and shrinked with the increase of the number of target dots. Finally, the distribution of spatial attention was estimated for each target dot condition under the assumption that the hit RT at each probe position reflects the amount of attention allocated there. Distributions estimated were cone-shaped, and the height and extent changed with the number of target dots. It was suggested that spatial limitation (i.e. spatial span of attention) in the processing of spatial positions can be explained by the notion of distribution of spatial attention.

Attention↗

Analysis of a distributed neural system involved in spatial information, novelty, and memory processing.

Perceiving a complex visual scene and encoding it into memory involves a hierarchical distributed network of brain regions, most notably the hippocampus (HIPP), parahippocampal gyrus (PHG), lingual gyrus (LNG), and inferior frontal gyrus (IFG). Lesion and imaging studies in humans have suggested that these regions are involved in spatial information processing as well as novelty and memory encoding; however, the relative contributions of these regions of interest (ROIs) are poorly understood. This study investigated regional dissociations in spatial information and novelty processing in the context of memory encoding using a 2 x 2 factorial design with factors Novelty (novel vs. repeated) and Stimulus (viewing scenes with rich vs. poor spatial information). Greater activation was observed in the right than left hemisphere; however, hemispheric effects did not differ across regions, novelty, or stimulus type. Significant novelty effects were observed in all four regions. A significant ROI x Stimulus interaction was observed - spatial information processing effects were largest effects in the LNG, significant in the PHG and HIPP and nonsignificant in the IFG. Novelty processing was stimulus dependent in the LNG and stimulus independent in the PHG, HIPP, and IFG. Analysis of the profile of Novelty x Stimulus interaction across ROIs provided evidence for a hierarchical independence in novelty processing characterized by increased dissociation from spatial information processing. Despite these differences in spatial information processing, memory performance for novel scenes with rich and poor spatial information was not significantly different. Memory performance was inversely correlated with right IFG activation, suggesting the involvement of this region in strategically flawed encoding effort. Stepwise regression analysis revealed that memory encoding accounted for only a small fraction of the variance (< 16%) in medial temporal lobe activation. The implications of these results for spatial information, novelty, and memory processing in each stage of the distributed network are discussed.

Adolescent↗

Dynamics of spatial frequency tuning in macaque V1.

Spatial frequency tuning in the lateral geniculate nucleus of the thalamus (LGN) and primary visual cortex (V1) differ substantially. LGN responses are largely low-pass in spatial frequency, whereas the majority of V1 neurons have bandpass characteristics. To study this transformation in spatial selectivity, we measured the dynamics of spatial frequency tuning using a reverse correlation technique. We find that a large proportion of V1 cells show inseparable responses in spatial frequency and time. In several cases, tuning becomes more selective over the course of the response, and the preferred spatial frequency shifts from low to higher frequencies. Many responses also show suppression at low spatial frequencies, which correlates with the increases in response selectivity and the shifts of preferred spatial frequency. These results indicate that suppression plays an important role in the generation of bandpass selectivity in V1.

Action Potentials↗

Accounting for the spatial rainfall variability in urban modelling applications.

In hydrological and hydrodynamic modelling of urban catchments, the spatial variability of rainfall is often neglected. This spatial variability encloses two aspects: (1) the spatial variability of the statistical properties of rainfall, and (2) the non-uniform spatial distribution of rainfall over the modelled catchments. In an ongoing research project for the Ministry of the Flemish Community (Belgium), the influence of this spatial rainfall variability on the results of modelling applications is studied. At the same time, most efficient methods to reduce this influence are determined. The results of the research can be applied directly in Flanders. They consist of a combination of unified IDF-relationships, spatial correction factors (generally applicable formulas), a stochastic simulation model for spatial rainfall (software) and a methodology for improving the spatial correction factors in a case-specific way by performing simulations with the model.

Cities↗

Neural systems underlying spatial language in American Sign Language.

A [(15)O]water PET experiment was conducted to investigate the neural regions engaged in processing constructions unique to signed languages: classifier predicates in which the position of the hands in signing space schematically represents spatial relations among objects. Ten deaf native signers viewed line drawings depicting a spatial relation between two objects (e.g., a cup on a table) and were asked either to produce a classifier construction or an American Sign Language (ASL) preposition that described the spatial relation or to name the figure object (colored red). Compared to naming objects, describing spatial relationships with classifier constructions engaged the supramarginal gyrus (SMG) within both hemispheres. Compared to naming objects, naming spatial relations with ASL prepositions engaged only the right SMG. Previous research indicates that retrieval of English prepositions engages both right and left SMG, but more inferiorly than for ASL classifier constructions. Compared to ASL prepositions, naming spatial relations with classifier constructions engaged left inferior temporal (IT) cortex, a region activated when naming concrete objects in either ASL or English. Left IT may be engaged because the handshapes in classifier constructions encode information about object type (e.g., flat surface). Overall, the results suggest more right hemisphere involvement when expressing spatial relations in ASL, perhaps because signing space is used to encode the spatial relationship between objects.

Adult↗

Effect of diffusion and spatially varying predation risk on the dynamics and equilibrium density of a predator-prey system.

Starting from natural planktonic systems, we present a new mechanism involving spatial heterogeneity, and develop a new spatial structure model of planktonic predation systems. Firstly, the effect of diffusion on the dynamics of the system is investigated. We find that diffusion of only prey or both prey and predator between different patches with different predation risk may stabilize the dynamics, depending on the flow rate. Only a medium flow rate can lead to the stability of the system. Too large a rate can cause the system to approach the non-spatial limit case of a well-mixed system. Too large a rate can cause the system to approach the non-spatial limit case as a well-mixed system, which is characterized by its strongly oscillatory dynamics. When only prey diffuse, the smaller the parameter f (the proportion of the patchy volume with larger predation risk to the total volume), the more stable the system. If both populations can diffuse, however, only medium and very small f values may stabilize the system. Also, the response of the spatially averaged equilibrium densities of the system to the increasing of the flow rate is examined. With increasing flow rate, the spatial-averaged equilibrium density of prey decreases, while that of predator depends on which species can diffuse. For the case of prey diffusion only, it first remains unchanged and then slightly decreases, while it increases for the case of combinations as the flow rate increases. Our results are, qualitatively, determined by the spatially heterogeneous mechanism that we propose, and further regulated by top-down forces. Of practical importance, the results reported here indicate that which species diffuse plays a key role in the ways in which diffusion influences the dynamics and the spatial-average equilibrium densities of the system responses to the flow rate's increasing.

Animals↗

Rat spatial memory tasks adapted for humans: characterization in subjects with intact brain and subjects with selective medial temporal lobe thermal lesions.

In the present paper we describe five tests, 3 of which were designed to be similar to tasks used with rodents. Results obtained from control subjects, patients with selective thermo-coagulation lesions to the medial temporal lobe and results from non-human primates and rodents are discussed. The tests involve memory for spatial locations acquired by moving around in a room, memory for objects subjects interacted with, or memory for objects and their locations. Two of the spatial memory tasks were designed specifically as analogs of the Morris water task and the 8-arm radial-maze tasks used with rats. The Morris water task was modeled by hiding a sensor under the carpet of a room (Invisible Sensor Task). Subjects had to learn its location by using an array of visual cues available in the room. A path integration task was developed in order to study the non-visual acquisition of a cognitive representation of the spatial location of objects. In the non-visual spatial memory task, we blindfolded subjects and led them to a room where they had to find 3 objects and remember their locations. We designed an object location task by placing 4 objects in a room that subjects observed for later recall of their locations. A recognition task, and a novelty detection task were given subsequent to the recall task. An 8-arm radial-maze was recreated by placing stands at equal distance from each other around the room, and asking subjects to visit each stand once, from a central point. A non-spatial working memory task was designed to be the non-spatial equivalent of the radial maze. Search paths recorded on the first trial of the Invisible Sensor Task, when subjects search for the target by trial and error are reported. An analysis of the search paths revealed that patients with lesions to the right or left hippocampus or parahippocampal cortex employed the same type of search strategies as normal controls did, showing similarities and differences to the search behavior recorded in rats. Interestingly, patients with lesions that included the right parahippocampal cortex were impaired relative to patients with lesions to the right hippocampus that spared the parahippocampal cortex, when recall of the sensor was tested after a 30 min delay (Bohbot et al. 1998). No differences were obtained between control subjects and patients with selective thermal lesions to the medial temporal lobe, when tested on the radial-maze, the non-spatial analogue to the radial-maze and the path integration tasks. Differences in methodological procedures, learning strategies and lesion location could account for some of the discrepant results between humans and non-human species. Patients with lesions to the right hippocampus, irrespective of whether the right parahippocampal cortex was spared or damaged, had difficulties remembering the particular configuration and identity of objects in the novelty detection of the object location task. This supports the role of the human right hippocampus for spatial memory, in this case, involving memory for the location of elements in the room; learning known to require the hippocampus in the rat.

Adolescent↗

[Spatial autocorrelation analysis on schistosomiasis cases and Oncomelania snails in three provinces of the lower reach of Yangtze River].

OBJECTIVE: To explore the spatial distribution of schistosomiasis cases and Oncomelania snails in the provinces of Jiangsu, Anhui and Jiangxi with the assistance of geographic information systems (GIS). METHODS: Epidemiological data of schistosomiasis in recent 20 years were collected, and the relevant GIS databases were established. The spatial autocorrelation analysis was carried out with ArcView 3. x, S-Plus, and Spatial Statistics software. RESULTS: Except for schistosomiasis cases in Jiangsu, the spatial distribution of schistosomiasis cases and Oncomelania snails in the three provinces were fitted to the spatial autocorrelation at a certain degree. Generally the autocorrelation coefficients (Moran's I) in Oncomelania snails were higher than that in schistosomiasis cases. CONCLUSION: Spatial autocorrelation analysis can be used to estimate the value of one variable in different spatial position, and it is a good way to find out the spatial cluster distribution in different stages.

Animals↗

Frequency-specific interaural level difference tuning predicts spatial response patterns of space-specific neurons in the barn owl inferior colliculus.

Space-specific neurons in the barn owl's inferior colliculus have spatial receptive fields (RFs) because of sensitivity to interaural time difference and frequency-specific interaural level difference (ILD). These neurons are assumed to be tuned to the frequency-specific ILDs occurring at their spatial RFs, but attempts to assess this tuning with traditional narrowband stimuli have had limited success. Indeed, tuning assessed in this manner, when processed via a linear model of spectral integration, typically explains only approximately half the variance in spatial response patterns. Here we report our findings that frequency-specific ILD tuning of space-specific neurons, when assessed from responses to broadband stimuli, predicted nearly 75% of the variance in spatial responses, using a linear model of spectral integration (p < 0.0001; n = 97 neurons). Furthermore, when we tested neurons using only those frequencies we found to be spatially relevant, we saw that their responses were similar to those elicited by broadband stimuli. When we used frequencies not identified as spatially relevant, such similarity was lacking. Furthermore, spectral components that elicited high firing rates when presented as narrowband stimuli were found in several cases to be irrelevant for or detrimental to the definition of spatial RFs. Thus, neurons achieved sharp spatial tuning by selecting for ILDs of a subset of spectral components in noise, some of which were not identified using narrowband stimuli.

Acoustic Stimulation↗

[Spatial variation of microbial properties in a creosote-contaminated soil].

By the methods of geostatistics, this paper studied the spatial variation of microbial biomass, microbial community structure and microbial activity in a creosote-contaminated soil. The microbial biomass was indicated by the total amount of 26 examined phospholipid fatty acids (totPLFA), the microbial community structure was characterized by the first two principal components (PC1 and PC2) of the PLFA patterns through subjecting the PLFAs to principal component analysis, and the total amount of CO2-C respired (C(re)) during incubation was used to describe the soil microbial activity. The results showed that most of the variables exhibited various degrees of spatial autocorrelation, and spherical models with nugget could fit their semivariograms. The estimated spatial dependence distances of the variables varied from 2.50 to 16.60 m. The PLFA PC1, totPLFA and C(re) displayed relatively high spatial dependences, their relative structural variance, i.e., the proportion of total variance that can be attributed to the spatial autocorrelation, being 82.3%, 79.6% and 64.7%, respectively, while PLFA PC2 was not spatially autocorrelated. The kriged maps showed that there were several hot spots with relatively high microbial biomass and high microbial activity located in the study site. Gram- negative bacteria characterized by PLFAs 16:1omega7t, cyl7:0, 18:1omega7 and cyl9:0 were the dominant community in these hot spots. The concentration and spatial distribution of polycyclic aromatic hydrocarbons as the main contaminants in the soil could be one of the important factors affecting the spatial variation of soil microbial properties.

Biodegradation, Environmental↗

[Development of spatial orientation during pilot training].

The problem of spatial orientation of pilots flying high-altitude aircraft is in the focus of present-day aviation medicine because of a growing number of accidents in the air. One of the productive lines of research is to study spatial orientation in terms of active formation and maintenance of its imagery in a complex environment. However investigators usually emphasize the role of visual (instrumental) information in the image construction, almost ignoring the sensorimotor component of spatial orientation. The theoretical analysis of the process of spatial orientation has facilitated the development of the concept assuming that the pattern of space perception changes with growing professional experience. The concept is based on an active approach to the essence, emergence, formation and variation in the pattern of sensory perception of space in man's consciousness. This concept asserts that as pilot's professional expertise increases, the pattern of spatial orientation becomes geocentric because a new system of spatial perception evolves which is a result of the development of a new (instrumental) type of motor activity in space. This finds expression in the fact that perception of spatial position inflight occurs when man has to resolve a new motor task--movement along a complex trajectory in the three-dimensional space onboard a flying vehicle. The meaningful structure of this problem which is to be implemented through controlling movements of the pilot acts as a factor that forms this new system of perception. All this underlies the arrangement of meaningful collection of instrumental data and detection of noninstrumental signals in the comprehensive perception of changes in the spatial position of a flying vehicle.

Aerospace Medicine↗

Rod light and dark adaptation influence cone-mediated spatial acuity.

The influence of rod light and dark adaptation upon cone mediated spatial acuity was studied in the near parafoveal retina of normal human observers. The luminance just necessary to detect squarewave test gratings of variable frequency provided an index of spatial acuity. Such thresholds were determined in the presence of background fields which were varied in luminance, shape, and size, or throughout the time period of dark adaptation. Spectral controls determined the type of photoreceptors influenced by all stimuli. Cone mediated spatial acuity is improved by presenting background fields too dim to directly affect cones, and is increasingly suppressed during the rod recovery stage of dark adaptation. These effects are small with spatial frequencies less than 4 c/deg but increase with spatial frequency to greater than 1 log10 unit with the highest spatial frequency examined, 21 c/deg. These influences upon cone mediated spatial vision reflect the state of long-term adaptation of rods in a large annular area surrounding the locus to which the test grating is presented. Our results emphasize the differing influences of long-term dark adaptation and prevailing luminance level upon visual acuity. Ironically, spatial acuity is optimized under dim light conditions by selectively light adapting the receptors most sensitive to feeble stimuli, the rods.

Adaptation, Ocular↗

Development of stereopsis depends upon contrast sensitivity and spatial tuning.

Various binocular functions such as disparity vergence, and stereopsis develop rapidly during the third to fifth month of life. This time frame coincides with the rapid postnatal development of visual acuity, contrast sensitivity and possibly the tuning of spatial channels. Recent studies of adult stereopsis reveal that small disparities near the stereo threshold are processed within spatial channels tuned above 2.5 cycles/deg. Sensitivity to these higher spatial frequencies develops during the 3-5 months of life. Adult studies also reveal that larger disparities are processed by spatial channels tuned to lower spatial frequencies. Tuning of these low spatial frequency channels may not be present until 3 months of age. Lack of spatial tuning prior to 3 months is predicted to be associated with a lack of disparity tuning as well as an inability to ignore false disparities in ambiguous or redundant stimuli such as random dot stereograms. These observations suggest that refractive anomalies such as anisometropia that limit high frequency spatial resolution and binocular integration can present a major obstacle to the postnatal development of binocular vision.

Adult↗

Emergence and characterization of sex differences in spatial ability: a meta-analysis.

Sex differences in spatial ability are widely acknowledged, yet considerable dispute surrounds the magnitude, nature, and age of first occurrence of these differences. This article focuses on 3 questions about sex differences in spatial ability: What is the magnitude of sex differences in spatial ability? On which aspects of spatial ability are sex differences found? and When, in the life span, are sex differences in spatial ability first detected? Implications for clarifying the linkage between sex differences in spatial ability and other differences between males and females are discussed. We use meta-analysis, a method for synthesizing empirical studies, to investigate these questions. Results of the meta-analysis suggest that sex differences arise on some types of spatial ability but not others, that large sex differences are found only on measures of mental rotation, that smaller sex differences are found on measures of spatial perception, and that, when sex differences are found, they can be detected across the life span.

Adolescent↗

Single-cell and spatial transcriptomic technologies for lung cancer tumor microenvironment analysis.

Lung cancer remains one of the leading causes of cancer-related mortality worldwide; beyond its rising incidence, its marked molecular heterogeneity and complex tumor microenvironment (TME) hinder treatment response and drive resistance, contributing directly to its high mortality rate. Single-cell RNA sequencing (scRNA-seq) and spatial transcriptomics (ST) provide complementary approaches for dissecting these features. scRNA-seq enables high-resolution analysis of cellular diversity and transcriptional states but requires tissue dissociation and therefore loses spatial context. In contrast, ST preserves tissue architecture and provides insights into how gene-expression programs within the TME are organized, although no currently available spatial platform combines whole-transcriptome coverage with true single-cell resolution over large tissue areas. Together, these technologies have enabled detailed mapping of tumor, immune and stromal populations and of their spatial interactions, revealing functionally distinct cellular niches that contribute to immune evasion, metastasis and response to therapy. In this narrative review we organize the primary literature around a single question, how spatially structured cellular ecosystems, rather than individual cell types, determine therapeutic response and resistance in lung cancer - and we explicitly separate observations that are reproducible across independent cohorts and platforms from those that remain confined to single studies. We further summarize the technical, analytical and logistic barriers that currently prevent spatially resolved signatures from entering routine diagnostic pathology. Understanding dysregulated pathways and spatially constrained intercellular communication within the TME helps identify candidate biomarkers and may support the identification of therapeutic approaches directed at tumor-intrinsic programs as well as at microenvironment-driven resistance mechanisms.

Cell-cell communication↗

Decoding tumor immune microenvironment heterogeneity by single-cell and spatial multi-omics: From immunotherapy resistance to translational biomarkers.

Immune checkpoint blockade has transformed cancer therapy, yet primary and acquired resistance remain major clinical challenges. Increasing evidence indicates that immunotherapy resistance cannot be fully explained by tumor-intrinsic alterations or conventional biomarkers such as PD-L1 expression, tumor mutational burden, or microsatellite instability. Instead, therapeutic response is shaped by the tumor immune microenvironment (TIME) as a heterogeneous, spatially organized, and dynamically evolving ecosystem. Single-cell omics has revealed diverse immune and stromal cell states, including progenitor and terminally exhausted T cells, suppressive myeloid programs, B-cell/TLS-associated immune-reactive states, and CAF-mediated exclusion phenotypes. Spatial transcriptomics, spatial proteomics, and imaging-based approaches further demonstrate that these cell states assemble into distinct immune niches, including immune-inflamed, T-cell-excluded, myeloid-suppressive, metabolic/hypoxic, and TLS-associated niches. These spatial ecosystems determine whether antitumor immune cells can access malignant cells, receive antigen-presenting support, or become restrained by stromal, vascular, metabolic, and myeloid barriers. In this review, we summarize how single-cell and spatial multi-omics redefine TIME heterogeneity in immunotherapy resistance, highlight ligand-receptor communication networks linking cell states to spatial immune dysfunction, and discuss emerging translational biomarkers for patient stratification. We further propose that future immunotherapy biomarkers should evolve from static single-marker assays toward longitudinal, spatially resolved, and interpretable multi-omics models that guide precision combination immunotherapy.

Humans↗