62 research outputs found

    Determinants of European and United States Unemployment

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    Molecular Community Analysis of Arbuscular Mycorrhizal Fungi in Roots of Geothermal Soils in Yellowstone National Park (USA)

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    To better understand adaptation of plants and their mycorrhizae to extreme environmental conditions, we analyzed the composition of communities of arbuscular mycorrhizal fungi (AMF) in roots from geothermal sites in Yellowstone National Park (YNP), USA. Arbuscular mycorrhizal fungi were identified using molecular methods including seven specific primer pairs for regions of the ribosomal DNA that amplify different subgroups of AMF. Roots of Dichanthelium lanuginosum, a grass only occurring in geothermal areas, were sampled along with thermal and nonthermal Agrostis scabra and control plants growing outside the thermally influenced sites. In addition, root samples of Agrostis stolonifera from geothermal areas of Iceland were analyzed to identify possible common mycosymbionts between these geographically isolated locations. In YNP, 16 ribosomal DNA phylotypes belonging to the genera Archaeospora, Glomus, Paraglomus, Scutellospora, and Acaulospora were detected. Eight of these phylotypes could be assigned to known morphospecies, two others have been reported previously in molecular studies from different environments, and six were new to science. The most diverse and abundant lineage was Glomus group A, with the most frequent phylotype corresponding to Glomus intraradices. Five of the seven phylotypes detected in a preliminary sampling in a geothermal area in Iceland were also found in YNP. Nonthermal vegetation was dominated by a high diversity of Glomus group A phylotypes while nonthermal plants were not. Using multivariate analyses, a subset of three phylotypes were determined to be associated with geothermal conditions in the field sites analyzed. In conclusion, AMF communities in geothermal soils are distinct in their composition, including both unique phylotypes and generalist fungi that occur across a broad range of environmental condition

    Root proteomic responses to heat stress in two Agrostis grass species contrasting in heat tolerance

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    Protein metabolism plays an important role in plant adaptation to heat stress. This study was designed to identify heat-responsive proteins in roots associated with thermotolerance for two C3 grass species contrasting in heat tolerance, thermal Agrostis scabra and heat-sensitive Agrostis stolonifera L. Plants were exposed to 20 °C (control), 30 C (moderate heat stress), or 40 °C (severe heat stress) in growth chambers. Roots were harvested at 2 d and 10 d after temperature treatment. Proteins were extracted and separated by two-dimensional polyacrylamide gel electrophoresis. Seventy protein spots were regulated by heat stress in at least one species. Under both moderate and severe heat stress, more proteins were down-regulated than were up-regulated, and thermal A. scabra roots had more up-regulated proteins than A. stolonifera roots. The sequences of 66 differentially expressed protein spots were identified using mass spectrometry. The results suggested that the up-regulation of sucrose synthase, glutathione S-transferase, superoxide dismutase, and heat shock protein Sti (stress-inducible protein) may contribute to the superior root thermotolerance of A. scabra. In addition, phosphoproteomic analysis indicated that two isoforms of fructose-biphosphate aldolase were highly phosphorylated under heat stress, and thermal A. scabra had greater phosphorylation than A. stolonifera, suggesting that the aldolase phosphorylation might be involved in root thermotolerance

    Intended Consequences Statement in Conservation Science and Practice

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    As the biodiversity crisis accelerates, the stakes are higher for threatened plants and animals. Rebuilding the health of our planet will require addressing underlying threats at many scales, including habitat loss and climate change. Conservation interventions such as habitat protection, management, restoration, predator control, trans location, genetic rescue, and biological control have the potential to help threatened or endangered species avert extinction. These existing, well-tested methods can be complemented and augmented by more frequent and faster adoption of new technologies, such as powerful new genetic tools. In addition, synthetic biology might offer solutions to currently intractable conservation problems. We believe that conservation needs to be bold and clear-eyed in this moment of great urgency

    Can we save large carnivores without losing large carnivore science?

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    CNRM-CM5 median daily SWE forecasts.

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    <p>Blue lines = Official 30 year SNOTEL daily normals (calculated as 1981–2010 daily medians), obtained from the Natural Resources Conservation Service. Orange Lines = CNRM-CM5 daily medians for 2031–2060. Red Lines = average of CNRM-CM5 SWE daily medians for 2061–2090. The CNRM-CM5 model forecast a greater loss of snow in early winter.</p

    Map showing Snow-telemetry (SNOTEL) weather stations in and near Yellowstone National Park.

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    <p>Left: Background shows average number of days per water year (October–September) with SWE greater than 0 cm. Right: Background shows average annual peak (greatest) SWE (cm). Data source = SNODAS [<a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0159218#pone.0159218.ref020" target="_blank">20</a>]. Both panels are averaged over water years ending 2005–2014, which was the length of record available for this data source. Gray areas = Lakes.</p

    Median annual peak SWE for 7 SNOTEL locations under the RCP 4.5 scenario.

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    <p>Historical (1990–2010) medians are calculated from historical SNOTEL weather station data. Mid- and late- 21<sup>st</sup> century values are model forecasts.</p

    Mean Absolute Error for modeled data from road points vs. modeled data from the most similar SNOTEL-containing location.

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    <p>Road points to the right of the dashed red line were excluded from further analysis. See <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0159218#sec002" target="_blank">Methods</a> for details of MAE calculations.</p
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