Integrating Academic and Non-Academic Instruction for Students with Emotional/Behavioral Disorders

Students with emotional/behavioral disorders exhibit a wide range of academic and behavioral problems. Not surprisingly, there is growing support for integrating instruction to address overlapping students\u27 needs in both areas. In this article, we discuss instructional variables that contribute to a positive classroom climate and that serve as setting events for more focused group-individual instructional programs. We draw on the accumulated research to identify common non-academic challenges that should be incorporated into those programs. We examine issues that relate to the efficacy of instruction and also the cultural and chronological age differences among students and how they relate to planning for instruction. Finally, we offer several forms that illustrate ways to combine academics and non-academics into a manageable instructional plan

Discovery of a [WO] central star in the planetary nebula Th 2-A

% context About 2500 planetary nebulae are known in our Galaxy but only 224 have central stars with reported spectral types in the Strasbourg-ESO Catalogue of Galactic Planetary Nebulae (Acker et al. 1992; Acker et al. 1996) % aims We have started an observational program aiming to increase the number of PN central stars with spectral classification. % methods By means of spectroscopy and high resolution imaging, we identify the position and true nature of the central star. We carried out low resolution spectroscopic observations at CASLEO telescope, complemented with medium resolution spectroscopy performed at Gemini South and Magellan telescopes. % results As a first outcome of this survey, we present for the first time the spectra of the central star of the PN Th 2-A. These spectra show emission lines of ionized C and O, typical in Wolf-Rayet stars. % conclusions We identify the position of that central star, which is not the brightest one of the visual central pair. We classify it as of type [WO 3]pec, which is consistent with the high excitation and dynamical age of the nebula.Comment: 3 pages and 2 figures. Paper recommended for publication in A&

Muscle Synergies Obtained from Comprehensive Mapping of the Cortical Forelimb Representation Using Stimulus Triggered Averaging of EMG Activity

This work is licensed under a Creative Commons Attribution 4.0 International License.Neuromuscular control of voluntary movement may be simplified using muscle synergies similar to those found using non-negative matrix factorization. We recently identified synergies in electromyography (EMG) recordings associated with both voluntary movement and movement evoked by high-frequency long-duration intracortical microstimulation applied to the forelimb representation of the primary motor cortex (M1). The goal of this study was to use stimulus-triggered averaging (StTA) of EMG activity to investigate the synergy profiles and weighting coefficients associated with poststimulus facilitation, as synergies may be hard-wired into elemental cortical output modules and revealed by StTA. We applied StTA at low (LOW, ∼15 μA) and high intensities (HIGH, ∼110 μA) to 247 cortical locations of the M1 forelimb region in two male rhesus macaques while recording the EMG of 24 forelimb muscles. Our results show that 10–11 synergies accounted for 90% of the variation in poststimulus EMG facilitation peaks from the LOW-intensity StTA dataset while only 4–5 synergies were needed for the HIGH-intensity dataset. Synergies were similar across monkeys and current intensities. Most synergy profiles strongly activated only one or two muscles; all joints were represented and most, but not all, joint directions of motion were represented. Cortical maps of the synergy weighting coefficients suggest only a weak organization. StTA of M1 resulted in highly diverse muscle activations, suggestive of the limiting condition of requiring a synergy for each muscle to account for the patterns observed

Elemental abundances of Galactic bulge planetary nebulae from optical recombination lines

(abridged) Deep long-slit optical spectrophotometric observations are presented for 25 Galactic bulge planetary nebulae (GBPNe) and 6 Galactic disk planetary nebulae (GDPNe). The spectra, combined with archival ultraviolet spectra obtained with the International Ultraviolet Explorer (IUE) and infrared spectra obtained with the Infrared Space Observatory (ISO), have been used to carry out a detailed plasma diagnostic and element abundance analysis utilizing both collisional excited lines (CELs) and optical recombination lines (ORLs). Comparisons of plasma diagnostic and abundance analysis results obtained from CELs and from ORLs reproduce many of the patterns previously found for GDPNe. In particular we show that the large discrepancies between electron temperatures (Te's) derived from CELs and from ORLs appear to be mainly caused by abnormally low values yielded by recombination lines and/or continua. Similarly, the large discrepancies between heavy element abundances deduced from ORLs and from CELs are largely caused by abnormally high values obtained from ORLs, up to tens of solar in extreme cases. It appears that whatever mechanisms are causing the ubiquitous dichotomy between CELs and ORLs, their main effects are to enhance the emission of ORLs, but hardly affect that of CELs. It seems that heavy element abundances deduced from ORLs may not reflect the bulk composition of the nebula. Rather, our analysis suggests that ORLs of heavy element ions mainly originate from a previously unseen component of plasma of Te's of just a few hundred Kelvin, which is too cool to excite any optical and UV CELs.Comment: 35 pages, 27 figures and 16 tables, accepted for publication in MNRA

The 600 yr eruptive history of Villarrica Volcano (Chile) revealed by annually laminated lake sediments

Lake sediments contain valuable information about past volcanic and seismic events that have affected the lake catchment, and they provide unique records of the recurrence interval and magnitude of such events. This study uses a multilake and multiproxy analytical approach to obtain reliable and high-resolution records of past natural catastrophes from similar to 600-yr-old annually laminated (varved) lake sediment sequences extracted from two lakes, Villarrica and Calafquen, in the volcanically and seismically active Chilean Lake District. Using a combination of micro-X-ray fluorescence (mu XRF) scanning, microfacies analysis, grain-size analysis, color analysis, and magnetic-susceptibility measurements, we detect and characterize four different types of event deposits (lacustrine turbidites, tephra-fall layers, runoff cryptotephras, and lahar deposits) and produce a revised eruption record for Villarrica Volcano, which is unprecedented in its continuity and temporal resolution. Glass geochemistry and mineralogy also reveal deposits of eruptions from the more remote Carran-Los Venados volcanic complex, Quetrupillan Volcano, and the Huanquihue Group in the studied lake sediments. Time-series analysis shows 112 eruptions with a volcanic explosivity index (VEI) >= 2 from Villarrica Volcano in the last similar to 600 yr, of which at least 22 also produced lahars. This significantly expands our knowledge of the eruptive frequency of the volcano in this time window, compared to the previously known eruptive history from historical records. The last VEI >= 2 eruption of Villarrica Volcano occurred in 1991. Based on the last similar to 500 yr, for which we have a complete record from both lakes, we estimate the probability of the occurrence of future eruptions from Villarrica Volcano and statistically demonstrate that the probability of a 22 yr repose period (anno 2013) without VEI >= 2 eruptions is <= 1.7%. This new perspective on the recurrence interval of eruptions and historical lahar activity will help improve volcanic hazard assessments for this rapidly expanding tourist region, and it highlights how lake records can be used to significantly improve historical eruption records in areas that were previously uninhabited

A comparative study between catalase gene therapy and the cardioprotector monohydroxyethylrutoside (MonoHER) in protecting against doxorubicin-induced cardiotoxicity in vitro

50) limited the possibility to increase catalase activity more than 3.5-fold, which was not enough to protect infected NeRCaMs against doxorubicin-induced cardiotoxicity and (2) confirms the efficacy of monoHER as a cardioprotector. Thus, the use of monoHER proves more suitable for the prevention of doxorubicin-induced cardiotoxicity than catalase gene transfer employing adenovirus vectors

The new cardioprotector Monohydroxyethylrutoside protects against doxorubicin-induced inflammatory effects in vitro

The new cardioprotector Monohydroxyethylrutoside protects against doxorubicin-induced inflammatory effects in vitro. Abou El Hassan MA, Verheul HM, Jorna AS, Schalkwijk C, van Bezu J, van der Vijgh WJ, Bast A. Department of Medical Oncology, Free University Medical Center, PO Box 7057, 1007 MB Amsterdam, The Netherlands. [email protected] Besides its cardiotoxic effect, doxorubicin also elicits inflammatory effects in vivo. 7-Monohydroxyethylrutoside (monoHER) has recently been used as a protector against doxorubicin-induced cardiotoxicity in vivo. It is not known yet whether monoHER can also protect against doxorubicin-induced inflammatory effects. The aim of the present study was (1) to illustrate the inflammatory effects of doxorubicin in vitro and (2) to evaluate a possibly protective effect of monoHER. In order to demonstrate the inflammatory effects of doxorubicin and the possible protection of monoHER, proliferating human umbilical cord vascular endothelial cells (HUVECs) were incubated with different concentrations of doxorubicin ranging from 12.5 to 600 nM with(out) 200 micro M monoHER. Resting (confluent) HUVECs were incubated with (0.5-25 micro M) doxorubicin with(out) monoHER (0.2-1.2 mM) and the viability of endothelial cells and their propensity to adhere to neutrophils were measured 24 h after treatment. The localisation of adhered neutrophils was determined with immunofluorescence microscopy. To further characterise the mechanism of doxorubicin-induced neutrophil adhesion, the expression of the HUVECs surface adhesion molecules was determined after doxorubicin treatment. Doxorubicin decreased the viability and proliferation capacity of HUVECs in a concentration-dependent manner. The proliferating HUVECs were much more sensitive to doxorubicin (IC(50)=60.0+/-20.8 nM) than resting cells (LC(50)=4.0+/-0.3 micro M). Doxorubicin also increased the adhesion of neutrophils reaching a plateau value at a doxorubicin concentration of > or =0.4 micro M (P=0.0113). The induced neutrophil adhesion was accompanied by overexpression of VCAM and E-selectin but not ICAM. Although monoHER did not reverse the effect of doxorubicin on the proliferation of endothelial cells, it significantly protected resting HUVECs against the cytotoxic effect of doxorubicin (< or =25 micro M, P<0.0015). In addition, monoHER completely protected against the stimulatory effect of doxorubicin on neutrophil adhesion, and inhibited the doxorubin-induced expression of VCAM and E-selectin on the surface of treated HUVECs. This study illustrates that monoHER, which protects against doxorubicin's cardiotoxic effect, can also protect against doxorubicin-induced inflammatory effects. These data prompt further investigation about the possible link between doxorubicin-induced inflammatory effects and its cardiotoxicity in viv

Pathophysiology of acute experimental pancreatitis: Lessons from genetically engineered animal models and new molecular approaches

The incidence of acute pancreatitis is growing and worldwide population-based studies report a doubling or tripling since the 1970s. 25% of acute pancreatitis are severe and associated with histological changes of necrotizing pancreatitis. There is still no specific medical treatment for acute pancreatitis. The average mortality resides around 10%. In order to develop new specific medical treatment strategies for acute pancreatitis, a better understanding of the pathophysiology during the onset of acute pancreatitis is necessary. Since it is difficult to study the early acinar events in human pancreatitis, several animal models of acute pancreatitis have been developed. By this, it is hoped that clues into human pathophysiology become possible. In the last decade, while employing molecular biology techniques, a major progress has been made. The genome of the mouse was recently sequenced. Various strategies are possible to prove a causal effect of a single gene or protein, using either gain-of-function (i.e., overexpression of the protein of interest) or loss-of-function studies (i.e., genetic deletion of the gene of interest). The availability of transgenic mouse models and gene deletion studies has clearly increased our knowledge about the pathophysiology of acute pancreatitis and enables us to study and confirm in vitro findings in animal models. In addition, transgenic models with specific genetic deletion or overexpression of genes help in understanding the role of one specific protein in a cascade of inflammatory processes such as pancreatitis where different proteins interact and co-react. This review summarizes the recent progress in this field. Copyright (c) 2005 S. Karger AG, Basel

FAM222B Is Not a Likely Novel Candidate Gene for Cerebral Cavernous Malformations

Cerebral cavernous malformations (CCMs) are prevalent slow-flow vascular lesions which harbour the risk to develop intracranial haemorrhages, focal neurological deficits, and epileptic seizures. Autosomal dominantly inherited CCMs were found to be associated with heterozygous inactivating mutations in 3 genes, CCM1(KRIT1), CCM2(MGC4607), and CCM3(PDCD10) in 1999, 2003 and 2005, respectively. Despite the availability of high-throughput sequencing techniques, no further CCM gene has been published since. Here, we report on the identification of an autosomal dominantly inherited frameshift mutation in a gene of thus far unknown function, FAM222B(C17orf63), through exome sequencing of CCM patients mutation-negative for CCM1-3. A yeast 2-hybrid screen revealed interactions of FAM222B with the tubulin cytoskeleton and STAMBP which is known to be associated with microcephaly-capillary malformation syndrome. However, a phenotype similar to existing models was not found, neither in fam222bb/fam222ba double mutant zebrafish generated by transcription activator-like effector nucleases nor in an in vitro sprouting assay using human umbilical vein endothelial cells transfected with siRNA against FAM222B. These observations led to the assumption that aberrant FAM222B is not involved in the formation of CCMs