Fire Effects on Three Trophic Levels in a Central Arkansas Grassland

We studied the effect of a late growing-season fire on the plant and foliar arthropod communities in a naturally occurring grassland. In central Arkansas, these grasslands are common on south-facing slopes where shallow soils and hot/dry weather conditions during the summer cannot support the growth of a forest community. Patches of grassland were burned in the autumn (4 November, late growing season), often the time of natural fires in Arkansas, and compared to unburned areas. Fire increased the biomass of forbs and decreased the biomass of grasses, although overall biomass was not different between treatments. Among the foliar arthropods, herbivores were significantly reduced by burning, especially the Homoptera. Carnivorous arthropods as a whole were not affected by burning, although spiders showed a small but significant reduction. The response of arthropods to fire occurred almost one year after the burn, showing that fire effects can be delayed for a substantial period of time. This experiment shows that fire occurring during the natural burning period in Arkansas can have substantial effects on grasslands communities. The response of plants in Arkansas is similar to that of plants in nearby grasslands on the Great Plains and southeastern United States which also show a great increase in forbs under late growing season burning regimes. The changes seen in this experiment demonstrate that the suppression of fire by humans has probably modified the structure of Arkansas grasslands. With the increasing use of fire as a management tool in Arkansas, changes to grassland systems are likely to be profound

Nanomechanics of Multiple Units in the Erythrocyte Membrane Skeletal Network

Erythrocytes undergo deformations when they transport O(2) and CO(2) across the membrane, yet the 3D nanomechanics of the skeletal network remains poorly understood. Expanding from our previous single isolated unit, we now simulate networks consisting of 1–10 concentric rings of repeating units in equibiaxial deformation. The networks are organized with (1) a 3D model for a single unit, (2) a wrap-around mode between Sp and actin protofilament in the intra-unit interaction, and (3) a random inter-unit connectivity. These assumptions permit efficient five-degrees-of-freedom (5DOF) simulations when up to 30 pN of radial forces are applied to the boundary spectrin (Sp) and the center and other units are analyzed. As 6 Sp balance their tensions, hexagonal units become irregular. While actin protofilaments remain tangent to the network, their yaw (Φ) angles change drastically with addition of neighboring units or an Sp unfolding. It is anticipated that during deformation, transmembrane complexes associated with the network move laterally through the lipid bilayer and increase the diffusion of molecules across the membrane. When protofilament/Sp sweeps under the lipid bilayer, they mix up the submembrane concentration gradient. Thus, the nanomechanics of actin protofilaments and Sp may enhance the transport of molecules during erythrocyte deformation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s10439-010-0040-4) contains supplementary material, which is available to authorized users

Your Path to Transplant: A randomized controlled trial of a tailored computer education intervention to increase living donor kidney transplant

Background: Because of the deceased donor organ shortage, more kidney patients are considering whether to receive kidneys from family and friends, a process called living donor kidney transplantation (LDKT). Although Blacks and Hispanics are 3.4 and 1.5 times more likely, respectively, to develop end stage renal disease (ESRD) than Whites, they are less likely to receive LDKTs. To address this disparity, a new randomized controlled trial (RCT) will assess whether Black, Hispanic, and White transplant patients’ knowledge, readiness to pursue LDKT, and receipt of LDKTs can be increased when they participate in the Your Path to Transplant (YPT) computer-tailored intervention. Methods/Design: Nine hundred Black, Hispanic, and White ESRD patients presenting for transplant evaluation at University of California, Los Angeles Kidney and Pancreas Transplant Program (UCLA-KPTP) will be randomly assigned to one of two education conditions, YPT or Usual Care Control Education (UC). As they undergo transplant evaluation, patients in the YPT condition will receive individually-tailored telephonic coaching sessions, feedback reports, video and print transplant education resources, and assistance with reducing any known socioeconomic barriers to LDKT. Patients receiving UC will only receive transplant education provided by UCLA-KPTP. Changes in transplant knowledge, readiness, pros and cons, and self-efficacy to pursue LDKT will be assessed prior to presenting at the transplant center (baseline), during transplant evaluation, and 4- and 8-months post-baseline, while completion of transplant evaluation and receipt of LDKTs will be assessed at 18-months post-baseline. The RCT will determine, compared to UC, whether Black, Hispanic, and White patients receiving YPT increase in their readiness to pursue LDKT and transplant knowledge, and become more likely to complete transplant medical evaluation and pursue LDKT. It will also examine how known patient, family, and healthcare system barriers to LDKT act alone and in combination with YPT to affect patients’ transplant decision-making and behavior. Statistical analyses will be performed under an intent-to-treat approach. Discussion: At the conclusion of the study, we will have assessed the effectiveness of an innovative and cost-effective YPT intervention that could be utilized to tailor LDKT discussion and education based on the needs of individual patients of different races in many healthcare settings. Trial Registration: ClinicalTrials.gov, number NCT02181114

Duke Ellington: Beyond Category KSU Symphony Orchestra with Jazz Ensemble I

The KSU Symphony Orchestra and Jazz Ensemble I team up for Duke Ellington: Beyond Category featuring Amy Smithwick, soprano and Jacob Sustaita, guest conductor. (Note: Principal viola for this concert is Dajon Carter, not Nathan Gay as listed.)https://digitalcommons.kennesaw.edu/musicprograms/2271/thumbnail.jp

Fire Effects on Three Trophic Levels in a Central Arkansas Grassland

We studied the effect of a late growing-season fire on the plant and foliar arthropod communities in a naturally occurring grassland. In central Arkansas, these grasslands are common on south-facing slopes where shallow soils and hot/dry weather conditions during the summer cannot support the growth of a forest community. Patches of grassland were burned in the autumn (4 November, late growing season), often the time of natural fires in Arkansas, and compared to unburned areas. Fire increased the biomass of forbs and decreased the biomass of grasses, although overall biomass was not different between treatments. Among the foliar arthropods, herbivores were significantly reduced by burning, especially the Homoptera. Carnivorous arthropods as a whole were not affected by burning, although spiders showed a small but significant reduction. The response of arthropods to fire occurred almost one year after the burn, showing that fire effects can be delayed for a substantial period of time. This experiment shows that fire occurring during the natural burning period in Arkansas can have substantial effects on grasslands communities. The response of plants in Arkansas is similar to that of plants in nearby grasslands on the Great Plains and southeastern United States which also show a great increase in forbs under late growing season burning regimes. The changes seen in this experiment demonstrate that the suppression of fire by humans has probably modified the structure of Arkansas grasslands. With the increasing use of fire as a management tool in Arkansas, changes to grassland systems are likely to be profound

Effects of antiplatelet therapy on stroke risk by brain imaging features of intracerebral haemorrhage and cerebral small vessel diseases: subgroup analyses of the RESTART randomised, open-label trial

Background Findings from the RESTART trial suggest that starting antiplatelet therapy might reduce the risk of recurrent symptomatic intracerebral haemorrhage compared with avoiding antiplatelet therapy. Brain imaging features of intracerebral haemorrhage and cerebral small vessel diseases (such as cerebral microbleeds) are associated with greater risks of recurrent intracerebral haemorrhage. We did subgroup analyses of the RESTART trial to explore whether these brain imaging features modify the effects of antiplatelet therapy

Phenotypic and transcriptomic analysis of peripheral blood plasmacytoid and conventional dendritic cells in early drug naïve rheumatoid arthritis

Objective: Dendritic cells (DCs) are key orchestrators of immune function. To date, rheumatoid arthritis (RA) researchers have predominantly focused on a potential pathogenic role for CD1c+ DCs. In contrast, CD141+ DCs and plasmacytoid DCs (pDCs) have not been systematically examined, at least in early RA. In established RA, the role of pDCs is ambiguous and, since disease duration and treatment both impact RA pathophysiology, we examined pDCs, and CD1c+ and CD141+ conventional DCs (cDCs), in early, drug-naïve RA (eRA) patients. Methods: We analyzed the frequency and phenotype of pDCs, CD1c+, and CD141+ DCs from eRA patients and compared findings with healthy controls. In parallel, we performed transcriptional analysis of >600 immunology-related genes (Nanostring) from peripheral blood pDCs, CD1c+ DCs, B cells, T cells, and monocytes. Results: All DC subsets were reduced in eRA (n = 44) compared with healthy controls (n = 30) and, for pDCs, this was most marked in seropositive patients. CD141+ and CD1c+ DCs, but not pDCs, had a comparatively activated phenotype at baseline (increased CD86) and CD1c+ DC frequency inversely associated with disease activity. All DC frequencies remained static 12 months after initiation of immunomodulatory therapy despite a fall in activation markers (e.g., HLA-DR, CD40). There was no association between the whole blood interferon gene signature (IGS) and pDC or CD1c+ DC parameters but an inverse association between CD141+ DC frequency and IGS was noted. Furthermore, IFN-I and IFN-III mRNA transcripts were comparable between eRA pDC and other leukocyte subsets (B cells, CD4+, and CD8+ T cells and monocytes) with no obvious circulating cellular source of IFN-I or IFN-III. Transcriptomic analysis suggested increased pDC and CD1c+ DC proliferation in eRA; pDC differentially expressed genes also suggested enhanced tolerogenic function, whereas for CD1c+ DCs, pro-inflammatory transcripts were upregulated. Discussion: This is the first detailed examination of DC subsets in eRA peripheral blood. Compared with CD1c+ DCs, pDCs are less activated and may be skewed toward tolerogenic functions. CD141+ DCs may be implicated in RA pathophysiology. Our findings justify further investigation of early RA DC biology