192 research outputs found
Effect of Extraction on Wood Density of Western Hemlock (Tsuga Heterophylla (RAF.) SARG.)
Extractives can account for between 1 to 20% of the oven-dry weight of wood of various tree species and can influence wood density values appreciably. Removing these chemical deposits (extraction) in wood samples can help establish a consistent baseline for comparing wood densities where extractives are expected to differ between sample parameters. Although western hemlock is a very important timber species in the Pacific Northwest, laboratories that determine wood density may or may not remove extractives prior to density assessment. Wood density values were compared before and after extraction for 19 young-growth western hemlock samples. Extraction was performed using 95% ethyl alcohol-toluene solutions. Ring density values averaged 0.045 g/cm3 lower for extracted samples compared to unextracted samples across rings. Slightly higher amounts of extractives were found at rings near the pith; however, a general consistency in extractive content existed among samples and along the radial profile
Tropolone Content of Increment Cores as an Indicator of Decay Resistance in Western Redcedar
The high decay resistance of western redeedar (Thuja plicata Donn) is due to the presence of toxic extractives, called tropolones, in the heartwood. Therefore, tropolone content may be used as an indicator of decay resistance. With increment core-sized samples of western redcedar heartwood, we used gas chromatography to measure tropolone content and soil block tests to assess decay resistance. Results showed that decay resistance was extremely variable at low tropolone levels, but was uniformly high at tropolone levels of 0.25% or greater. Analyzing tropolone content of western redeedar increment cores is a useful way to assess decay resistance of standing trees
Comentarios a la ponencia "Igualdades, desigualdades y derechos", presentada por Mirta Lobato
Teniendo en cuenta -como advierte Mirta Lobato a los comentaristas- que cuando habla de desigualdades en su ponencia se refiere a que "el trabajo es el eje articulador de estas reflexiones", y sin dejar de reconocer la importancia que cabe a los otros temas y sujetos sobre los que tan bien desarrolla su exposición, quiero centrarme en un grupo que estoy estudiando desde hace unos años, como es el de los inmigrantes limítrofes a la Argentina de fin de siglo XX e inicios del XXI. Para ello, voy a analizar brevemente -como así lo exigen las reglas del comentario- a estos sujetos sociales, a quienes, como también ella afirma, ya los habríamos de encontrar censalmente a inicios del siglo pasado, aunque su visibilidad fuera menor porque aún no habían arribado a Buenos Aires; es decir, al escenario donde "las cosas suceden".Fil: Benencia, Roberto Rodolfo. Universidad de Buenos Aires; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentin
Differential expression of CD300a/c on human TH1 and TH17 cells
<p>Abstract</p> <p>Background</p> <p>Human memory CD4<sup>+ </sup>T cells can be either CD300a/c<sup>+ </sup>or CD300a/c<sup>- </sup>and subsequent analyses showed that CD4<sup>+ </sup>effector memory T (T<sub>EM</sub>) cells are mostly CD300a/c<sup>+</sup>, whereas CD4<sup>+ </sup>central memory T (T<sub>CM</sub>) cells have similar frequencies of CD300a/c<sup>+ </sup>and CD300a/c<sup>- </sup>cells.</p> <p>Results</p> <p>Extensive phenotypical and functional characterization showed that in both T<sub>CM </sub>and T<sub>EM </sub>cells, the CD300a/c<sup>+ </sup>subset contained a higher number of T<sub>H</sub>1 (IFN-γ producing) cells. Alternatively, T<sub>H</sub>17 (IL-17a producing) cells tend to be CD300a/c<sup>-</sup>, especially in the T<sub>EM </sub>subset. Further characterization of the IL-17a<sup>+ </sup>cells showed that cells that produce only this cytokine are mostly CD300a/c<sup>-</sup>, while cells that produce IL-17a in combination with other cytokines, especially IFN-γ, are mostly CD300a/c<sup>+</sup>, indicating that the expression of this receptor is associated with cells that produce IFN-γ. Co-ligation of the TCR and CD300a/c in CD4<sup>+ </sup>T cells inhibited Ca<sup>2+ </sup>mobilization evoked by TCR ligation alone and modulated IFN-γ production on T<sub>H</sub>1 polarized cells.</p> <p>Conclusion</p> <p>We conclude that the CD300a/c receptors are differentially expressed on human T<sub>H</sub>1 and T<sub>H</sub>17 cells and that their ligation is capable of modulating TCR mediated signals.</p
Investigations into free tropospheric new particle formation in the central Canadian arctic during the winter/spring transition as part of TOPSE
In this paper, we investigate the role of in situ new particle production in the central Canadian sub-Arctic and Arctic as part of the TOPSE experiment. Airborne measurements conducted primarily in the free troposphere were made from 50° to 90°W longitude and 60° to 85°N latitude during the period from February to May 2000. Data pertinent to this paper include 3–4 nm diameter (Dp) particles, ultrafine condensation nuclei (Dp \u3e 3 nm), fine particles (0.2 \u3c Dp \u3c 3 μm), and the possible nucleation precursor, sulfuric acid, and its precursor, sulfur dioxide. For data averaged over this period, most species showed little evidence for a latitudinal trend. Fine aerosol number concentrations, however, showed a slight increase with latitude. The evolution of various species concentrations over the period of the study show that fine particles also had a consistent temporal trend, increasing at all altitudes from February to May, whereas sulfur dioxide at the surface tended to peak in late March. Ultrafine condensation nuclei and 3–4 nm particles showed no temporal trends. Little evidence for in situ new particle production was observed during the study, except for one atypical event where SO2concentrations were 3.5 ppbv, 2 orders of magnitude higher than typical levels. This paper cannot address the question of whether the observed condensation nuclei were produced in situ by a low particle production rate or transported from lower latitudes
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Time and distance to clear wood in pruned red alder saplings
This paper was published in: Deal, R.L. and C.A. Harrington, eds. 2006. Red alder—a state of knowledge. General Technical Report PNW-GTR-669. Portland, OR: U.S. Department of Agriculture, Pacific Northwest Research Station. 150 p.Pruning trials in young alder stands were sampled to
evaluate response to pruning. Effects of pruning (1) live
branches on different dates, and (2) dead branches with
or without damaging the branch collar were assessed on
trees pruned in 3- and 6-year-old plantations, respectively.
Six years after pruning, stem sections were collected and
dissected in the longitudinal-radial plane to expose the
center of the stem and branch stub. Ring counts and linear
measurements were made for various boundaries or points,
including time of pruning, stub length, defect, and beginning
of clear wood formation. Pruning during the growing
season and, to a lesser extent, late in the growing season
when leaf abscission was beginning, resulted in shorter
times and distances to formation of clear wood (2.1 years,
14.5 mm) than pruning in the dormant season or just prior
to the beginning of the growing season (2.6 years, 18.6
mm). Cutting the branch collar on dead branches led to
shorter times and distances to clear wood (2.8 years, 21.9
mm) than intentionally avoiding such wounding (3.5 years,
24.8 mm); these differences were associated with shorter
branch stubs as there were no differences in the amount
of defect. Epicormic branching was minimal in the two
pruning studies, averaging less than one branch per tree in
the date of pruning test and only two branches per tree in the
branch collar wounding study. Assessments for comparable
unpruned trees indicated that times to form clear wood after
branch death would be markedly greater and that epicormic
branching was equal to or greater than that determined for
pruned trees. Although statistically significant differences
occurred among different pruning dates and with branch
collar wounding, the decision to prune or not prune is of
much greater practical importance, regardless of when (date)
or how it is done. Such pruning decisions can be made by
using this information on time and distance to clear wood
in economic analyses developed with available data on tree
growth, log volume, lumber recovery, pruning costs, and
price differentials for clear vs. knotty wood.Keywords: biology and ecology, inventory, economics, Alnus rubra, history, mixed-species stands, silviculture, pruning, plantation establishment, supplyKeywords: biology and ecology, inventory, economics, Alnus rubra, history, mixed-species stands, silviculture, pruning, plantation establishment, suppl
Interpreting genotype-by-environment interaction for biomass production in hybrid poplars under short-rotation coppice in Mediterranean environments
Understanding genotype × environment interaction (GEI) is crucial to optimize the deployment of clonal material to field conditions in short‐rotation coppice poplar plantations. Hybrid poplars are grown for biomass production under a wide range of climatic and edaphic conditions, but their adaptive performance in Mediterranean areas remains poorly characterized. In this work, site regression (SREG) and factorial regression mixed models are combined to gain insight into the nature and causes underlying GEI for biomass production of hybrid poplar clones. SREG addresses the issue of clonal recommendation in multi‐environment trials through a biplot representation that visually identifies superior genotypes. Factorial regression, alternatively, involves a description of clonal reaction to the environment in terms of physical variables that directly affect productivity. Initially, SREG aided in identifying cross‐over interactions that often involved hybrids of different taxonomic background. Factorial regression then selected latitude, mean temperature of the vegetative period (MTVP) and soil sand content as main site factors responsible for differential clonal adaptation. Genotypic responses depended strongly on taxonomic background: P. deltoides Bartr. ex Marsh. × P. nigra L. clones showed an overall positive sensitivity to increased MTVP and negative sensitivity to increased sand content, whereas the opposite occurred for P. trichocarpa Torr. & Gray × P. deltoides clones; the three‐cross hybrid [(P. deltoides × P. trichocarpa) × P. nigra] often displayed an intermediate performance. This information can contribute toward the identification and biological understanding of adaptive characteristics relevant for poplar breeding in Mediterranean conditions and facilitate clonal recommendation at eco‐regional level.This research was funded by MINECO (Spain) throughout the
project RTA2008-00025-C02-01 and RTA2011-00006-00-00. We
also acknowledge the collaboration of project AGL2009-11006.
We would like to thank the public company SOMACYL for
hosting one of the experimental plots. We are also grateful to
Juan Pablo de la Iglesia and Ana Parras for their technical support
throughout the experiment
Location, location, location: considerations when using lightweight drones in challenging environments
Lightweight drones have emerged recently as a remote sensing survey tool of choice for ecologists, conservation practitioners and environmental scientists. In published work, there are plentiful details on the parameters and settings used for successful data capture, but in contrast there is a dearth of information describing the operational complexity of drone deployment. Information about the practices of flying in the field, whilst currently lacking, would be useful for others embarking on new drone-based investigations. As a group of drone-piloting scientists, we have operated lightweight drones for research in over 25 projects, in over 10 countries, and in polar, desert, coastal and tropical ecosystems, with many hundreds of hours of flying experience between us. The purpose of this paper was to document the lesser-reported methodological pitfalls of drone deployments so that other scientists can understand the spectrum of considerations that need to be accounted for prior to, and during drone survey flights. Herein, we describe the most common challenges encountered, alongside mitigation and remediation actions that increase the chances of safe and successful data capture. Challenges are grouped into the following categories: (i) pre-flight planning, (ii) flight operations, (iii) weather, (iv) redundancy, (v) data quality, (vi) batteries. We also discuss the importance of scientists undertaking ethical assessment of their drone practices, to identify and mitigate potential conflicts associated with drone use in particular areas. By sharing our experience, our intention is that the paper will assist those embarking on new drone deployments, increasing the efficacy of acquiring high-quality data from this new proximal aerial viewpoint.This work was supported by the Natural Environment Research Council [NE/K570009815], [NE/K500902/1] (to AMC), [NE/M016323/1] (to IHM-S), [NE/570009815] (to JPD) and the UK Technology Strategy Board [TS/K00266X/1] (to KA). JS and KA were partly supported by the European Space Agency contract No. 4000117644/16/NL/FF/gp
Phospholipase C–mediated hydrolysis of PIP2 releases ERM proteins from lymphocyte membrane
Mechanisms controlling the disassembly of ezrin/radixin/moesin (ERM) proteins, which link the cytoskeleton to the plasma membrane, are incompletely understood. In lymphocytes, chemokine (e.g., SDF-1) stimulation inactivates ERM proteins, causing their release from the plasma membrane and dephosphorylation. SDF-1–mediated inactivation of ERM proteins is blocked by phospholipase C (PLC) inhibitors. Conversely, reduction of phosphatidylinositol 4,5-bisphosphate (PIP2) levels by activation of PLC, expression of active PLC mutants, or acute targeting of phosphoinositide 5-phosphatase to the plasma membrane promotes release and dephosphorylation of moesin and ezrin. Although expression of phosphomimetic moesin (T558D) or ezrin (T567D) mutants enhances membrane association, activation of PLC still relocalizes them to the cytosol. Similarly, in vitro binding of ERM proteins to the cytoplasmic tail of CD44 is also dependent on PIP2. These results demonstrate a new role of PLCs in rapid cytoskeletal remodeling and an additional key role of PIP2 in ERM protein biology, namely hydrolysis-mediated ERM inactivation
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