347 research outputs found

    Climate change in the Kola Peninsula, Arctic Russia, during the last 50 years from meteorological observations

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    Abstract The authors provide a detailed climatology and evaluation of recent climate change in the Kola Peninsula, Arctic Russia, a region influenced by both the North Atlantic and Arctic Oceans. The analysis is based on 50 years of monthly surface air temperature (SAT), precipitation (PPN), and sea level pressure (SLP) data from 10 meteorological stations for 1966–2015. Regional mean annual SAT is ~0°C: the moderating effect of the ocean is such that coastal (inland) stations have a positive (negative) value. Examined mean annual PPN totals rise from ~430 mm in the northeast of the region to ~600 mm in the west. Annual SAT in the Kola Peninsula has increased by 2.3° ± 1.0°C over the past 50 years. Seasonally, statistically significant warming has taken place in spring and fall, although the largest trend has occurred in winter. Although there has been no significant change in annual PPN, spring has become significantly wetter and fall drier. The former is associated with the only significant seasonal SLP trend (decrease). A positive winter North Atlantic Oscillation (NAO) index is generally associated with a warmer and wetter Kola Peninsula whereas a positive Siberian high (SH) index has the opposite impact. The relationship between both the NAO and SH and the SAT is broadly coherent across the region whereas their relationship with PPN varies markedly, although none of the relationships is temporally invariant. Reduced sea ice in the Barents and White Seas and associated circulation changes are likely to be the principal drivers behind the observed changes.We thank Valery Demin for supplying the SAT and PPN data for Lovozero prior to 1985. In addition, we thank the staff at the various data portals described in Section 3 for their time and effort in making the data available. GJM is supported by the UK Natural Environment Research Council (NERC) through the British Antarctic Survey research program Polar Science for Planet Earth. RMV is funded by NERC PhD studentship NE/L002507/1.This is the author accepted manuscript. It first appeared from the American Meteorological Society at http://dx.doi.org/10.1175/JCLI-D-16-0179.1

    What colour is penguin guano?

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    The identification and quantification of Antarctic Pygoscelis penguin colonies depends increasingly on recognition of the characteristic optical properties of guano deposits, but almost all knowledge of these properties until now has been compromised by resolution and atmospheric propagation effects. Here we present hyperspectral reflectance data in the range 350–2500 nm, collected in situ from fresh guano deposits in Pygoscelis penguin colonies on Signy Island, South Orkney Islands. The period of data collection included the transition from predominantly white guano to the pink coloration characteristic of a krill-rich diet. The main identifiable features in the spectra are a broad absorption feature centred around 550 nm, responsible for the pink coloration and identified with the pigment astaxanthin, as well as several water absorption features. Variations in these features are responsible for differentiation between spectra. From these results we propose two spectral indices suitable for use with satellite data, one of which responds to the presence of astaxanthin in the guano and the other to water. Our results do not allow us to differentiate between penguin species from their guano, but do suggest that the breeding phenology of Pygoscelis penguins could be determined from a time series of multispectral imagery.The fieldwork necessary for this work was supported by BAS through a Collaborative Gearing Scheme award CGS-97 to W.G. Rees and P.N. Trathan, and the ASD FieldSpec Pro was made available through an award (ref. 696.0614) from the UK NERC Field Spectroscopy Facility. We acknowledge with gratitude the support and companionship of the entire staff of the BAS research station at Signy, and especially of M. Jobson, the Base Commander. J.A. Brown is supported by a NERC PhD studentship NE/L501633/1

    What parathyroid hormone levels should we aim for in children with stage 5 chronic kidney disease; what is the evidence?

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    The bone disease that occurs as a result of chronic kidney disease (CKD) is not only debilitating but also linked to poor growth and cardiovascular disease. It is suspected that abnormal bone turnover is the main culprit for these poor outcomes. Plasma parathyroid hormone (PTH) levels are used as a surrogate marker of bone turnover, and there is a small number of studies in children that have attempted to identify the range of PTH levels that correlates with normal bone histology. It is clear that high PTH levels are associated with high bone turnover, although the range is wide. However, the ability of PTH levels to distinguish between low and normal bone turnover is less clear. This is an important issue, because current guidelines for calcium and phosphate management are based upon there being an “optimum” range for PTH. This editorial takes a critical look at the evidence upon which these recommendations are based

    The data paper: a mechanism to incentivize data publishing in biodiversity science

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    <p/> <p>Background</p> <p>Free and open access to primary biodiversity data is essential for informed decision-making to achieve conservation of biodiversity and sustainable development. However, primary biodiversity data are neither easily accessible nor discoverable. Among several impediments, one is a lack of incentives to data publishers for publishing of their data resources. One such mechanism currently lacking is recognition through conventional scholarly publication of enriched metadata, which should ensure rapid discovery of 'fit-for-use' biodiversity data resources.</p> <p>Discussion</p> <p>We review the state of the art of data discovery options and the mechanisms in place for incentivizing data publishers efforts towards easy, efficient and enhanced publishing, dissemination, sharing and re-use of biodiversity data. We propose the establishment of the 'biodiversity data paper' as one possible mechanism to offer scholarly recognition for efforts and investment by data publishers in authoring rich metadata and publishing them as citable academic papers. While detailing the benefits to data publishers, we describe the objectives, work flow and outcomes of the pilot project commissioned by the Global Biodiversity Information Facility in collaboration with scholarly publishers and pioneered by Pensoft Publishers through its journals <it>Zookeys</it>, <it>PhytoKeys</it>, <it>MycoKeys</it>, <it>BioRisk</it>, <it>NeoBiota</it>, <it>Nature Conservation</it> and the forthcoming <it>Biodiversity Data Journal</it>. We then debate further enhancements of the data paper beyond the pilot project and attempt to forecast the future uptake of data papers as an incentivization mechanism by the stakeholder communities.</p> <p>Conclusions</p> <p>We believe that in addition to recognition for those involved in the data publishing enterprise, data papers will also expedite publishing of fit-for-use biodiversity data resources. However, uptake and establishment of the data paper as a potential mechanism of scholarly recognition requires a high degree of commitment and investment by the cross-sectional stakeholder communities.</p

    Phenylthiourea Specifically Reduces Zebrafish Eye Size

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    Phenylthiourea (PTU) is commonly used for inhibiting melanization of zebrafish embryos. In this study, the standard treatment with 0.2 mM PTU was demonstrated to specifically reduce eye size in larval fish starting at three days post-fertilization. This effect is likely the result of a reduction in retinal and lens size of PTU-treated eyes and is not related to melanization inhibition. This is because the eye size of tyr, a genetic mutant of tyrosinase whose activity is inhibited in PTU treatment, was not reduced. As PTU contains a thiocarbamide group which is presented in many goitrogens, suppressing thyroid hormone production is a possible mechanism by which PTU treatment may reduce eye size. Despite the fact that thyroxine level was found to be reduced in PTU-treated larvae, thyroid hormone supplements did not rescue the eye size reduction. Instead, treating embryos with six goitrogens, including inhibitors of thyroid peroxidase (TPO) and sodium-iodide symporter (NIS), suggested an alternative possibility. Specifically, three TPO inhibitors, including those that do not possess thiocarbamide, specifically reduced eye size; whereas none of the NIS inhibitors could elicit this effect. These observations indicate that TPO inhibition rather than a general suppression of thyroid hormone synthesis is likely the underlying cause of PTU-induced eye size reduction. Furthermore, the tissue-specific effect of PTU treatment might be mediated by an eye-specific TPO expression. Compared with treatment with other tyrosinase inhibitors or bleaching to remove melanization, PTU treatment remains the most effective approach. Thus, one should use caution when interpreting results that are obtained from PTU-treated embryos

    Short tandem repeat profiling: part of an overall strategy for reducing the frequency of cell misidentification

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    The role of cell authentication in biomedical science has received considerable attention, especially within the past decade. This quality control attribute is now beginning to be given the emphasis it deserves by granting agencies and by scientific journals. Short tandem repeat (STR) profiling, one of a few DNA profiling technologies now available, is being proposed for routine identification (authentication) of human cell lines, stem cells, and tissues. The advantage of this technique over methods such as isoenzyme analysis, karyotyping, human leukocyte antigen typing, etc., is that STR profiling can establish identity to the individual level, provided that the appropriate number and types of loci are evaluated. To best employ this technology, a standardized protocol and a data-driven, quality-controlled, and publically searchable database will be necessary. This public STR database (currently under development) will enable investigators to rapidly authenticate human-based cultures to the individual from whom the cells were sourced. Use of similar approaches for non-human animal cells will require developing other suitable loci sets. While implementing STR analysis on a more routine basis should significantly reduce the frequency of cell misidentification, additional technologies may be needed as part of an overall authentication paradigm. For instance, isoenzyme analysis, PCR-based DNA amplification, and sequence-based barcoding methods enable rapid confirmation of a cell line’s species of origin while screening against cross-contaminations, especially when the cells present are not recognized by the species-specific STR method. Karyotyping may also be needed as a supporting tool during establishment of an STR database. Finally, good cell culture practices must always remain a major component of any effort to reduce the frequency of cell misidentification

    ER-Alpha-cDNA As Part of a Bicistronic Transcript Gives Rise to High Frequency, Long Term, Receptor Expressing Cell Clones

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    Within the large group of Estrogen Receptor alpha (ERα)-negative breast cancer patients, there is a subgroup carrying the phenotype ERα−, PR−, and Her2−, named accordingly “Triple-Negative” (TN). Using cell lines derived from this TN group, we wished to establish cell clones, in which ERα is ectopically expressed, forming part of a synthetic lethality screening system. Initially, we generated cell transfectants expressing a mono-cistronic ERα transcription unit, adjacent to a separate dominant selectable marker transcription unit. However, the yield of ERα expressing colonies was rather low (5–12.5%), and only about half of these displayed stable ectopic ERα expression over time. Generation and maintenance of such cell clones under minimal exposure to the ERα ligand, did not improve yield or expression stability. Indeed, other groups have also reported grave difficulties in obtaining ectopic expression of ERα in ERα-deficient breast carcinoma cells. We therefore switched to transfecting these cell lines with pERα-IRES, a plasmid vector encoding a bicistronic translation mRNA template: ERα Open Reading Frame (ORF) being upstream followed by a dominant-positive selectable marker (hygroR) ORF, directed for translation from an Internal Ribosome Entry Site (IRES). Through usage of this bicistronic vector linkage system, it was possible to generate a very high yield of ERα expressing cell clones (50–100%). The stability over time of these clones was also somewhat improved, though variations between individual cell clones were evident. Our successful experience with ERα in this system may serve as a paradigm for other genes where ectopic expression meets similar hardships
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