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81.
This article presents a case study of a marketing audit of the Lee County Library System, a rural public library system located in southwest Georgia. Marketing audits are an underutilized but needed tool for public libraries. In this audit, the library system’s mission, goals, environments, community and employee demographics, and a strengths/weakness/opportunities/threats (SWOT) analysis were evaluated, resulting in several recommendations. These recommendations include a new mission statement, regular SWOT analyses, and potential market segments for targeted library services. Through this case study, the complexities, challenges, and opportunities unique to rural public libraries can be understood.  相似文献   
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This study uses longitudinal data from the Project on Human Development in Chicago Neighborhoods (PHDCN) to examine the effects of exposure to school violence, community violence, child abuse, and parental intimate partner violence (IPV) on youths’ subsequent alcohol and marijuana use. We also examine the cumulative effects of being exposed to violence across these domains. Longitudinal data were obtained from 1,655 adolescents and their primary caregivers participating in the PHDCN. The effects of adolescents’ exposure to various forms of violence across different life domains were examined relative to adolescents’ frequency of alcohol and marijuana use three years later. Multivariate statistical models were employed to control for a range of child, parent, and family risk factors. Exposure to violence in a one-year period increased the frequency of substance use three years later, though the specific relationships between victimization and use varied for alcohol and marijuana use. Community violence and child abuse, but not school violence or exposure to IPV, were predictive of future marijuana use. None of the independent measures of exposure to violence significantly predicted future alcohol use. Finally, the accumulation of exposure to violence across life domains was detrimental to both future alcohol and marijuana use. The findings support prior research indicating that exposure to multiple forms of violence, across multiple domains of life, negatively impacts adolescent outcomes, including substance use. The findings also suggest that the context in which exposure to violence occurs should be considered in future research, since the more domains in which youth are exposed to violence, the fewer “safe havens” they have available. Finally, a better understanding of the types of violence youth encounter and the contexts in which these experiences occur can help inform intervention efforts aimed at reducing victimization and its negative consequences.  相似文献   
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The present study examined the influence of schooling during children's first and second years of preschool for children who experienced different amounts of preschool (i.e., one or two years), but who were essentially the same chronological age. Children (n = 76) were tested in the fall and spring of the school year using measures of self-regulation, decoding, letter knowledge, and vocabulary. Using hierarchical linear modeling (HLM), preschool was not associated with children's development of self-regulation in either year. For decoding and letter knowledge, children finishing their second year of preschool had higher scores, although both groups of children grew similarly during the school year. Thus, our results suggest that the first and second years of preschool are both systematically associated with decoding and letter knowledge gains, and the effects are cumulative (two years predicted greater gains overall than did one year of preschool). Finally, children's chronological age, and not whether they experienced one versus two years of preschool, predicted children's vocabulary and self-regulation outcomes. Implications for preschool curricula and instruction are discussed, including the increasing emphasis on literacy learning prior to kindergarten entry and the need to address self-regulation development along with academic learning.  相似文献   
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The UK engineering and technology (E&T) sector is male-dominated, with women facing various cultural and structural barriers in entering and developing their careers within it. Existing research in this area has focused on women’s recruitment or retaining women in employment, but little has addressed women’s transition to industry through the higher education (HE) system. This paper therefore explores women’s experiences of HE in E&T, focusing particularly on the gendered help and support women were found to receive, as well as possible causes and consequences of this behaviour. The research adopts a qualitative design, using semi-structured interviews with women E&T students. The gendered help women received is shown to be something of a ‘poisoned chalice’; although there are sometimes short-term benefits, this is likely to hinder women from progressing in their careers at the same rate as their male peers.  相似文献   
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A vacuum compatible microfluidic reactor, SALVI (System for Analysis at the Liquid Vacuum Interface), was employed for in situ chemical imaging of live biofilms using time-of-flight secondary ion mass spectrometry (ToF-SIMS). Depth profiling by sputtering materials in sequential layers resulted in live biofilm spatial chemical mapping. Two-dimensional (2D) images were reconstructed to report the first three-dimensional images of hydrated biofilm elucidating spatial and chemical heterogeneity. 2D image principal component analysis was conducted among biofilms at different locations in the microchannel. Our approach directly visualized spatial and chemical heterogeneity within the living biofilm by dynamic liquid ToF-SIMS.Mapping how metabolic pathways are interconnected and controlled at the subcellular scale within dynamic living systems continues to present a grand scientific challenge. Biofilms, consisting of aggregations of bacterial cells and extracellular polymeric substance (EPS), present an important avenue for deciphering complex microbial communities. During biofilm formation, cells assemble in a secreted polymer milieu of polysaccharides, proteins, glycolipids, and DNA.1,2 Microfluidics provides unprecedented control over flow conditions, accessibility to real-time observation, high-throughput testing, and mimics in vivo biological environments.3 An understanding of the mechanism underlying biofilm formation and the design of advanced microfluidic experiments could address challenges such as interpreting microbial community interactions, biofouling, and resistance to antimicrobial chemicals. However, only a handful of biofilm studies used microfluidic approaches that provided hydrated chemical imaging at high spatial resolution.4–7 Most studies utilized confocal microscopy,4 FTIR spectroscopy,5 or other approaches (e.g., high density interdigitated capacitors7) for biofilm monitoring. Imaging mass spectrometry has been demonstrated in biofilm studies.8,9 A coupled microfluidic-imaging mass spectrometry approach would provide the chemical molecular spatial mapping needed to better address the scientific challenge of biofilms.Recently, we developed a portable microfluidic reactor, System for Analysis at the Liquid Vacuum Interface (SALVI),10,11 which overcame the grand challenge of studying liquids with high volatility and liquid interfaces using surface sensitive vacuum instruments. SALVI enables direct imaging of liquid surfaces using electron or ion/molecular based vacuum techniques. Our microfluidic approach used a polydimethylsiloxane (PDMS) microchannel fully enclosed with a thin silicon nitride (SiN) membrane (100 nm thick). For visualization, 2 μm diameter holes were opened in the SiN membrane in vacuo. These detection windows were dynamically drilled using the time-of-flight secondary ion mass spectrometry (ToF-SIMS) primary ion beam (e.g., Bi+).12Unlike liquid sample holders for transmission electron microscopy and scanning transmission electron microscopy, SALVI is self-contained and portable.13 As a result, it can potentially be used in many finely focused analytical tool with minimal adaptation.10 The analytical performance of SALVI has been demonstrated with a variety of analytes ranging from biology to material sciences.14,15 Unlike most microfluidic applications that are only suitable under ambient conditions (e.g., separations, cell and small amount sample manipulation, and thermal flow-sensors),16–18 SALVI is compatible with both in situ ambient and in vacuo spectroscopy analysis and imaging.19 Biofilms have been successfully cultivated inside the microfluidic channel and imaged using correlative confocal laser scanning microscopy (CLSM) and ToF-SIMS.20Our approach opens a new avenue to study biological sample in their natural state. Although ToF-SIMS has been widely used for providing molecular signatures of organic and biological molecules in complex biological systems21,22 or lipid spatial mapping,23 the vacuum-based ToF-SIMS generally requires solid (either dried24 or cryo treated25) samples. Here, we report ToF-SIMS two dimensional (2D) and three dimensional (3D) chemical images of hydrated biofilms. In situ time and space-resolved identifications of fatty acid (FA) fragments characteristic of Shewanella are illustrated by 3D images reconstructed from the ToF-SIMS depth profile time series. Principal component analysis (PCA) further elucidates biofilm chemical and spatial heterogeneity and shows the key chemical component at different depth and location of the biofilm including the biofilm-surface attachment interface.For all growth experiments, two samples were cultured simultaneously. At days 5 and 6, one sample was harvested for immediate analysis, respectively, using a ToF-SIMS V spectrometer (IONTOF GmbH, Münster, Germany). Similar results were obtained from both samples, because the biofilm-attachment surface was probed. For consistency, only day 6 data are shown here, while additional data are provided in the supplementary material.28 2D and 3D image visualizations were obtained using the IONTOF instrument software. PCA was performed using MATLAB R2012a (MathWorks, Inc., Natick, MA, USA). 2D images of .bif format were converted and integrated into a matrix. Data were pretreated by normalization to total ions, square root transformation, and then mean centering.26 For m/z spectra PCA, unit mass peaks from m/z 199 to m/z 255 were used (see Figure S-228). Unit mass peaks from m/z 1–300 were also used and results are comparable (see Figure S-328). Five characteristic FA peaks (m/z 199, 213, 227, 241, and 255, corresponding to C12, C13, C14, C15, and C16 FAs) were used in image PCA.27 Images representing each PC were reconstructed from the score matrix using the red, green, and blue (RGB) color scale.Using depth profiling, we drilled through the SiN membrane and collected depth-resolved images of the live biofilm (Figure 1(a)). Our analysis of the negative ToF-SIMS spectra after SiN punch-through showed Shewanella FA fragments in the m/z 195–255 range.20 From the depth profile time series, we selected five regions (highlighted as I, II, III IV, and V) within the FA m/z range to visualize 2D spatially resolved images collected for 46 s (1000 scans) before (I), during (II), or after (III, IV, V) SiN membrane punch-through.20 When false color 2D images of FA fragments characteristic of Shewanella biofilms were selected from the dynamic depth profiling data, differences were observed (Figure 1(b)) among the five regions. Furthermore, the biofilm images after SiN membrane punch-through (III, IV, V) displayed variations across the 2 μm diameter surfaces, with C12 (m/z 199) being distributed across regions III, IV, and V and C15 (m/z 241) FAs mostly in region V (see Figure S-4 for additional FA images28). This suggested that depth-resolved chemical heterogeneities were present in the biofilm. To illustrate, we reconstructed the 2D images from depth profiling data within the biofilm region (from the beginning of III through the end of V) and show spatially resolved 3D chemical images within the entire sample (Figure 1(c) and movies S1-S328). The reconstructed 3D images revealed the heterogeneous spatial distribution overlay for C12 (red) and C15 (green) FAs during 302 s biofilm depth profiling from day 5 (Figure S-528) and day 6 (Figure 1(c)).Open in a separate windowFIG. 1.(a) ToF-SIMS depth profiling of the day 6 biofilm attached to the SiN membrane in the microfluidic channel. Five regions representing sample before SiN punch-through (I) during punch-through (II) or within the biofilm region (III, IV, and V) are illustrated. (b) 2D false color images of day 6 biofilm FAs at the five time regions highlighted in (a). (c) Reconstructed 3D day 6 biofilm images showing FA fragment distributions within the entire biofilm region (III–V, 302 s). The time axis represents depth profiling from near the SiN surface into the biofilm. (d) Spectra PCA score plot of day 6 biofilm showing the differences and similarities among selected five regions (m/z 199–255). A 95% confidence limit for each region was defined by an ellipse with the same color to the corresponding region clusters. (e) Loadings of PC1 and PC2 corresponding to (d) and the plot of PC variance contributions.Spectral PCA was used to analyze the m/z spectra. The deepest region (V) into the biofilm was the most different from the other two biofilm regions (III and IV), further confirming the heterogeneities observed in the 2D images (e.g., C12 and C15 FA fragments) contributing most to this spatial difference. In addition, C12 FA fragments played a key role in the biofilms imaged near the SiN membrane attachment surface (III and IV). When inspected individually, C12 FAs were observed throughout the entire biofilm region, suggesting that C12 FA fragments may play a role in biofilm attachment to a surface and they may be main components of EPS throughout the biofilm. In contrast, C15 FAs were more abundant deeper within the biofilm, indicating that they may be more relevant to bacteria cells themselves.Uniform sputtering rate was assumed during depth profiling. To better determine the depth and shape of the SIMS ionization crater, AFM measurements were collected using an agarose sample in the SALVI reactor as a proxy for the biofilms (Figure S-628). The AFM results showed that the 100 nm SiN was drilled through and confirmed that the biofilm interface was probed by ToF-SIMS. Ideally, real-time correlative AFM and ToF-SIMS measurements will be needed due to the self-healing property of biofilms. However, such capability is currently under development.To further analyze chemical differences within biofilms, we performed ToF-SIMS depth profiling at three locations along the microchannel; namely, the inlet, center, and outlet as illustrated in Figure S-1(b).28 At each location, we defined the five regions described in Figure 1(a), and 2D image PCA analysis was conducted on the biofilm region (from the beginning of III through the end of V) to visualize the chemical distributions on day 6. Figure 2(a) shows the loading plots for the m/z peaks that contribute to each PC image (Figure 2(b)). The first three PCs explained 93.79% of the variance within the data. For PC1, the strongest positive loading fragments were C12 and C15 FAs, which are the bright red areas in three PC1 images. The C12 FAs were the main contributor to the green regions in the PC2 image. The strongest loading for PC3 in blue was C14 FAs. Compared to PC1 and PC2, PC3 played a limited contribution to the overall spatial distribution discrimination. The merged images give a demonstration of chemical spatial distribution of key components of biofilms in the liquid microenvironment.Open in a separate windowFIG. 2.(a) Image PCA loading plots illustrating the contribution of each FA peak in the day 6 biofilm at three locations within the microfluidic channel. The variance contributions of each PC are shown at the bottom. (b) Reconstructed false-color 2D PCA images in RGB corresponding to each PC scores at these locations along the microfluidic channel. The RGB composite images of the three key PCs are depicted in the bottom. Only data within the 2 μm diameter circle were considered in analysis.Our results show that SALVI and liquid ToF-SIMS studies of live biofilms offer dynamic, depth-resolved chemical mapping and produce 2D and 3D visualizations of spatial heterogeneity within a biofilm. Chemical imaging of biofilms near the attachment interface can enhance our understanding of biofilm formation in environmental, medical, and industrial settings. Our approach provides a universal portable platform and enables in situ probing of complex living biological systems potentially across multiple time and space scales. Because of the portability and vacuum compatibility, SALVI offers a valuable linkage with proteomic mass spectrometry via microfluidics and a nondestructive package for integrative in situ analysis of live biological systems in system biology.  相似文献   
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Intimate partner violence, sexual violence, and stalking are pervasive in the United States, and college women are disproportionately affected by this power‐based personal violence (PBPV). Title IX mandates that colleges and universities offer support services to trauma survivors, and college counselors should be prepared to meet this need. Therefore, this article serves to explore a diverse assortment of trauma‐informed counseling techniques, based in feminist theory, for college counselors working with PBPV survivors.  相似文献   
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