Double jeopardy: Intimate partner violence vulnerability among emerging adult women through lenses of race and sexual orientation.

Objective: Intimate partner violence (IPV) remains a public health concern for women age 18-25. While much is known about the IPV risk and experiences of heterosexual women, little is known about the IPV risk and experiences of their LGBTQ + counterparts and any contributions of multiple marginalization in such risk. This study examines the emotional, physical, and sexual intimate partner violence (IPV) vulnerability of emerging adult college women with and without multiple minority statuses (e.g., women with both racial/ethnic and sexual minority identities). Participants: Participants were 9,435 women ages 18-25 from the National College Health Assessment (NCHA). Results: Findings demonstrate that being a sexual minority increases risk vulnerability for all forms of IPV, regardless of race. Conclusions: The risk for college women with multiple marginalized identities is exponentially greater than either their White or heterosexual counterparts. Implications for colleges/universities, university counseling centers and professionals, and future research directions are discussed.

Direct Brain Stimulation Modulates Encoding States and Memory Performance in Humans.

People often forget information because they fail to effectively encode it. Here, we test the hypothesis that targeted electrical stimulation can modulate neural encoding states and subsequent memory outcomes. Using recordings from neurosurgical epilepsy patients with intracranially implanted electrodes, we trained multivariate classifiers to discriminate spectral activity during learning that predicted remembering from forgetting, then decoded neural activity in later sessions in which we applied stimulation during learning. Stimulation increased encoding-state estimates and recall if delivered when the classifier indicated low encoding efficiency but had the reverse effect if stimulation was delivered when the classifier indicated high encoding efficiency. Higher encoding-state estimates from stimulation were associated with greater evidence of neural activity linked to contextual memory encoding. In identifying the conditions under which stimulation modulates memory, the data suggest strategies for therapeutically treating memory dysfunction.

Partial characterization of the Sox2+ cell population in an adult murine model of digit amputation.

Tissue regeneration in response to injury in adult mammals is generally limited to select tissues. Nonmammalian species such as newts and axolotls undergo regeneration of complex tissues such as limbs and digits via recruitment and accumulation of local and circulating multipotent progenitors preprogrammed to recapitulate the missing tissue. Directed recruitment and activation of progenitor cells at a site of injury in adult mammals may alter the default wound-healing response from scar tissue toward regeneration. Bioactive molecules derived from proteolytic degradation of extracellular matrix (ECM) proteins have been shown to recruit a variety of progenitor cells in vitro and in vivo to the site of injury. The present study further characterized the population of cells accumulating at the site of injury after treatment with ECM degradation products in a well-established model of murine digit amputation. After a mid-second phalanx digit amputation in 6-8-week-old adult mice, treatment with ECM degradation products resulted in the accumulation of a heterogeneous population of cells, a subset of which expressed the transcription factor Sox2, a marker of pluripotent and adult progenitor cells. Sox2+ cells were localized lateral to the amputated P2 bone and coexpressed progenitor cell markers CD90 and Sca1. Transgenic Sox2 eGFP/+ and bone marrow chimeric mice showed that the bone marrow and blood circulation did not contribute to the Sox2+ cell population. The present study showed that, in addition to circulating progenitor cells, resident tissue-derived cells also populate at the site of injury after treatment with ECM degradation products. Although future work is necessary to determine the contribution of Sox2+ cells to functional tissue at the site of injury, recruitment and/or activation of local tissue-derived cells may be a viable approach to tissue engineering of more complex tissues in adult mammals.

Aphids alter host-plant nitrogen isotope fractionation.

Plant sap-feeding insects and blood-feeding parasites are frequently depleted in (15)N relative to their diet. Unfortunately, most fluid-feeder/host nitrogen stable-isotope studies simply report stable-isotope signatures, but few attempt to elucidate the mechanism of isotopic trophic depletion. Here we address this deficit by investigating the nitrogen stable-isotope dynamics of a fluid-feeding herbivore-host plant system: the green peach aphid, Myzus persicae, feeding on multiple brassicaceous host plants. M. persicae was consistently more than 6‰ depleted in (15)N relative to their hosts, although aphid colonized plants were 1.5‰ to 2.0‰ enriched in (15)N relative to uncolonized control plants. Isotopic depletion of aphids relative to hosts was strongly related to host nitrogen content. We tested whether the concomitant aphid (15)N depletion and host (15)N enrichment was coupled by isotopic mass balance and determined that aphid (15)N depletion and host (15)N enrichment are uncoupled processes. We hypothesized that colonized plants would have higher nitrate reductase activity than uncolonized plants because previous studies had demonstrated that high nitrate reductase activity under substrate-limiting conditions can result in increased plant δ(15)N values. Consistent with our hypothesis, nitrate reductase activity in colonized plants was twice that of uncolonized plants. This study offers two important insights that are likely applicable to understanding nitrogen dynamics in fluid-feeder/host systems. First, isotopic separation of aphid and host depends on nitrogen availability. Second, aphid colonization alters host nitrogen metabolism and subsequently host nitrogen stable-isotope signature. Notably, this work establishes a metabolic framework for future hypothesis-driven studies focused on aphid manipulation of host nitrogen metabolism.