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961.
University students named a 72-ms masked target word that was preceded by two 120-ms consecutively presented words, a prime word followed by a distractor. In Experiment 1, all words were in lowercase letters, whereas in Experiment 2, the target word was changed to uppercase letters. In both experiments there was an accuracy and latency cost (repetition blindness: RB) when the prime was the same word as the target, with the cost much less severe in Experiment 2 than in Experiment 1. A low-frequency distractor impaired target identification compared with a high-frequency distractor. Distractor frequency interacted with target frequency such that high-frequency targets preceded by low-frequency distractors had the lowest accuracy. The results are consistent with a frequency-dependent competition for access to working memory among briefly displayed words. However, there was no clear evidence that effects of target repetition on interword competition play a role in RB. The effects of a letter case change for the target are consistent with a contribution of token distinctiveness to word-order recovery in the intervening-word priming task. 相似文献
962.
963.
Michael D. Robinson Jessica L. Bair Tianwei Liu Matthew J. Scott Ian B. Penzel 《Sex roles》2017,77(3-4):272-286
Men often score higher than women do on traits or tendencies marked by hostile dominance. The purpose of the present research was to contribute to an understanding of these gender differences. Four studies (total N?=?494 U.S. undergraduates) administered a modified animal preference test in which participants could choose to be predator or prey animals, but not labeled as such. Men were consistently more interested in being predator animals than women were, displaying a sort of hostile dominance in their projective preferences. Predator self-identifications, in turn, mediated gender differences in outcomes related to hostile dominance. Studies 1 and 2 provided initial evidence for this model in the context of variations in interpersonal arrogance, and Studies 3 and 4 extended the model to nonverbal displays and daily life prosociality, respectively. The findings indicate that gender differences in hostile dominance are paralleled by gender differences in preferring to think about the self in predator-like terms. Accordingly, the findings provide new insights into aggressive forms of masculine behavior. 相似文献
964.
A fairly robust finding in the deception literature is that lie-tellers show more negative emotion than truth-tellers. Ekman (1985), however, has reasoned that a specific type of negative emotion - anger - is especially difficult to feign and therefore should be more prevalent in truth-tellers who are falsely accused of a transgression than in lie-tellers who are guilty. To our knowledge, Ekman’s prediction has not yet been empirically tested. By comparing the verbal and nonverbal cues associated with truths and lies across a number of lie-eliciting situations, we demonstrate that truth-tellers accused of a wrongdoing do show more anger, both verbally and nonverbally, than lie-tellers accused of the same act, but only in situations where students choose to commit a transgression (or not) and actually believe themselves to be in trouble. Results underlie the importance of taking into consideration the type of lie being told in order to accurately predict deceptive cues. 相似文献
965.
According to the action-specific perception account, perception is a function of optical information and the perceiver's ability to perform the intended action. While most of the evidence for the action-specific perception account is on spatial perception, in the current experiments we examined similar effects in the perception of speed. Tennis players reproduced the time the ball traveled from the feeder machine to when they hit it. The players judged the ball to be moving faster on trials when they hit the ball out-of-bounds than on trials where they successfully hit the ball in-bounds. Follow-up experiments in the laboratory showed that participants judged virtual balls to be moving slower when they played with a bigger paddle in a modified version of Pong. These studies suggest that performance and task ease influence perceived speed. 相似文献
966.
Four studies examined why women appear to be less likely than men to lift weights, despite the documented health benefits. An archival analysis (“Study 1”) pointed to a cultural dissociation between women and strength-related exercise goals. Furthermore, a study of women in a university in the mid-Atlantic United States who envisioned lifting weights in public expressed greater evaluation concerns than those who envisioned doing aerobic exercise (“Study 2”); moreover, greater evaluation concerns seemed to deter them from weight lifting. These findings helped to shed light upon gender-differentiated patterns of gym equipment use (“Study 3a”) and reports of psychological discomfort in gyms (“Study 3b”). This work begins to illuminate the sociocultural context of women’s avoidance of certain types of exercise. 相似文献
967.
Christopher T. H. Liang Anisha Nathwani Sarah Ahmad Jessica K. Prince 《Journal of multicultural counseling and development》2010,38(2):77-87
The relationship between coping strategies used by South Asian American women and subjective well‐being (SWB) was studied. Second‐generation women were found to use more support compared with 1st‐generation women. Problem‐solving coping was inversely related to age. Avoidance coping was found to predict SWB when controlling for age and generational status. Se estudió la relación entre las estrategias de afrontamiento empleadas por mujeres americanas surasiáticas y el bienestar subjetivo (SWB, por sus siglas en inglés). Se descubrió que las mujeres de segunda generación emplean más apoyos que los que emplearon las mujeres de primera generación. El afrontamiento basado en la resolución de problemas fue inversamente proporcional a la edad. También se halló que el afrontamiento basado en la evitación puede predecir el SWB, cuando se controlan los datos de edad y estatus generacional. 相似文献
968.
Despite much psychological research regarding jury decision making, surprisingly little is known about the deliberation process
that gives rise to jury verdicts. We review classic jury decision-making research regarding the importance of deliberation
and more recent research, investigating deliberation and hung juries, that challenges the view that deliberation does not
have an important impact on verdicts. We advocate greater attention to potential cognitive processes during deliberation that
might explain the transition between predeliberation preferences and a jury’s ultimate verdict. We then review cognitive work
in the group context generally, and the jury context specifically, illustrating the promise of a cognitive perspective on
jury deliberation. Finally, we identify cognitive phenomena likely to be particularly valuable in illuminating deliberation
behavior. 相似文献
969.
Shauna M. Stark Michael A. Yassa Craig E.L. Stark 《Learning & memory (Cold Spring Harbor, N.Y.)》2010,17(6):284-288
Rodent studies have suggested that “pattern separation,” the ability to distinguish among similar experiences, is diminished in a subset of aged rats. We extended these findings to the human using a task designed to assess spatial pattern separation behavior (determining at time of test whether pairs of pictures shown during the study were in the same spatial locations). Using a standardized test of word recall to divide healthy aged adults into impaired and unimpaired groups relative to young performance, we demonstrate that aged impaired adults are biased away from pattern separation and toward pattern completion, consistent with the rodent studies.Memory impairment is a common complaint among aging individuals, yet the variability within the aging population is great in both rats (Gallagher et al. 2006; Robitsek et al. 2008) and humans (Hilborn et al. 2009). A rodent model of aging (Gallagher et al. 2006; Wilson et al. 2006) has demonstrated that ∼50% of healthy rats qualify as cognitively “impaired” by scoring outside the range of the young performance in a standard protocol (Gallagher et al. 1993). The other half, the “unimpaired” rats, perform on par with young adults, demonstrating a natural degree of variability in cognitive aging. In this study, we sought to capitalize on the variability observed in the aging of both rats and humans in a study of spatial pattern separation.One source of variability in memory performance is hypothesized to be tied to changes in the input to the dentate gyrus (DG), which has been shown in the rat to be affected by the aging process. Smith et al. (2000) reported a selective impairment in layer II entorhinal input into the DG and CA3 regions of the hippocampus in rats with cognitive impairment. Similarly, the number of synapses in the outer receiving layer of DG was reduced in autopsied aged brains and correlated with earlier performance on a delayed recall task (Scheff et al. 2006). Finally, in a human imaging study, Small et al. (2002) observed that 60% of their aging sample demonstrated diminished MRI signal in the hippocampal region (including the DG) and also had a greater decline in memory performance. These findings support the notion that changes in the DG associated with aging may affect memory performance.The DG may be particularly important for the computations that underlie pattern separation (Treves and Rolls 1994; McClelland et al. 1995; Norman and O''Reilly 2003). “Pattern separation” refers to the process by which similar inputs are stored as distinct, nonoverlapping representations. In contrast, “pattern completion” refers to the process by which an existing representation can be reinstated by the presentation of a partial or degraded cue. Numerous studies in the rodent have identified the importance of the DG for pattern separation using electrophysiological methods (Leutgeb et al. 2004, 2005, 2007; Leutgeb and Leutgeb 2007), immediate early gene expression (Vazdarjanova and Guzowski 2004), lesions (Lee et al. 2005; Gilbert and Kesner 2006; Goodrich-Hunsaker et al. 2008), and even genetic manipulations (Cravens et al. 2006; Kubik et al. 2007; McHugh et al. 2008). Human neuroimaging has also recently identified activity in the DG (and CA3 regions of the hippocampus) in an object pattern separation task (Kirwan and Stark 2007; Bakker et al. 2008).Given the importance of the DG in pattern separation and its vulnerability to changes that occur with aging, studies have begun to examine pattern separation in older adults. Our laboratory has designed a task to examine object-based pattern separation performance in humans (Kirwan and Stark 2007). In this task, pictures of objects were presented either once or repeatedly throughout the task. Critically, some of the items presented were lures that were similar but not identical to previously shown items. The overlapping features of the lures more heavily engaged pattern separation processes. In young adults, functional magnetic resonance imaging (fMRI) activity in the DG was sensitive to the lures, indicating a role in pattern separation processes in both an explicit (Kirwan and Stark 2007) and implicit (Bakker et al. 2008) version of this task. Toner et al. (2009) used the explicit version of this task to demonstrate that older adults showed a greater tendency to identify lures as “old” (repeated) relative to young adults. These findings were also recently replicated in our laboratory (Yassa et al., in press), with the additional demonstration that older adults exhibit greater fMRI CA3/DG activity for the lures during both encoding and retrieval.Since object-based pattern separation appears to be modulated by the DG in humans, we wondered if these findings could be extended to spatial pattern separation. Rodent studies have demonstrated that the DG has a particular role in spatial pattern separation (Gilbert et al. 2001; Kesner et al. 2004). Specifically, Hunsaker et al. (2008) placed rats with localized DG lesions in an environment with two objects spaced 60 cm apart. When the animals were later placed in the same environment with the same objects now placed 40 cm apart, DG-lesioned animals (unlike control animals) did not re-explore the objects or environment. These data suggest that the DG-lesioned rats were not able to discriminate between the training and test environments. That is, they were impaired in spatial pattern separation. Since converging evidence suggests that one feature of the aging process can be characterized as a DG knockdown, we modified this task design for humans to test spatial pattern separation performance in older adults. While the Hunsaker et al. (2008) task emphasized the distance between the two objects as the source of interference creating a greater need for pattern separation, the paradigm presented here moves an object in any direction, changing both the distance and the angle (i.e., changing more of the spatial relations). We posit that this amount of movement (close, medium, or far) may place similar demands on spatial pattern separation processes as in the rodent task.The present study included 20 young adults (mean age 19.9 yr, range 18–27 yr) and 30 aged adults (mean age 70.4 yr, range 59–80 yr). Aged adults completed a battery of standardized neuropsychological tests, including the Mini-Mental State Exam (Folstein et al. 1975), Rey Auditory–Verbal Learning Task (RAVLT) (Rey 1941), Digit Span, Vocabulary, and Matrices subtests from the Wechsler Adult Intelligence Scale III (Wechsler 1997). The Vocabulary and Matrices scores were entered into a weighted formula along with age, gender, and education to derive estimated IQ scores (Schoenberg et al. 2003). All aged participants scored within the normal age-adjusted ranges on these measures and were cognitively intact. Younger adults also completed the RAVLT and scored within the normal age-adjusted range. These data are presented in Table Young Aged (AU) Aged (AI) Unimpaired Impaired Years of age 19.9 (2.4) 69.1 (5.2) 72.9 (4.1) Years of education 14.1 (1.7)a 16.7 (1.8) 15.5 (2.9) Gender (male/female) 3M/17F 6M/14F 5M/5F RAVLT total performance 53.5 (6.7) 56.2 (6.4) 43.4 (6.1)b RAVLT immediate performance 12.1 (1.9) 12.2 (1.5) 8.3 (1.9)b RAVLT delay performance 11.8 (1.4) 11.8 (1.6) 6.5 (1.7)b Estimated IQ – 120.8 (5.5) 115 (6.7)b Digit span performance – 18.9 (4.5) 17 (3.8) Mini-Mental State examination – 28.6 (0.9) 28.3 (0.9)