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991.
992.
Adam Felton Joern Fischer David B. Lindenmayer Rebecca Montague-Drake Arianne R. Lowe Debbie Saunders Annika M. Felton Will Steffen Nicola T. Munro Kara Youngentob Jake Gillen Phil Gibbons Judsen E. Bruzgul Ioan Fazey Suzi J. Bond Carole P. Elliott Ben C. T. Macdonald Luciana L. Porfirio Martin Westgate Martin Worthy 《Biodiversity and Conservation》2009,18(8):2243-2253
Recent reviews of the conservation literature indicate that significant biases exist in the published literature regarding
the regions, ecosystems and species that have been examined by researchers. Despite the global threat of climatic change,
similar biases may be occurring within the sub-discipline of climate-change ecology. Here we hope to foster critical thought
and discussion by considering the directions taken by conservation researchers when addressing climate change. To form a quantitative
basis for our perspective, we assessed 248 papers from the climate change literature that considered the conservation management
of biodiversity and ecosystems. We found that roughly half of the studies considered climate change in isolation from other
threatening processes. We also found that the majority of surveyed scientific publications were conducted in the temperate
forests of Europe and North America. Regions such as Latin America that are rich in biodiversity but may have low adaptive
capacity to climate change were not well represented. We caution that such biases in research effort may be distracting our
attention away from vulnerable regions, ecosystems and species. Specifically we suggest that the under-representation of research
from regions low in adaptive capacity and rich in biodiversity requires international collaboration by those experienced in
climate-change research, with researchers from less wealthy nations who are familiar with local issues, ecosystems and species.
Furthermore, we caution that the propensity of ecologists to work in essentially unmodified ecosystems may fundamentally hamper
our ability to make useful recommendations in a world that is experiencing significant global change. 相似文献
993.
Dmitri Demidov Susann Hesse Annegret Tewes Twan Rutten Jörg Fuchs Raheleh Karimi Ashtiyani Sandro Lein reas Fischer Gunter Reuter Andreas Houben 《The Plant journal : for cell and molecular biology》2009,59(2):221-230
The enzymological properties of AtAurora1, a kinase responsible for the cell cycle-dependent phosphorylation of histone H3 at S10, and its cross-talk with other post-translational histone modifications, were determined. In vitro phosphorylation of H3S10 by AtAurora1 is strongly increased by K9 acetylation, and decreased by K14 acetylation and T11 phosphorylation. However, S10 phosphorylation activity is unaltered by mono-, di- or trimethylation of K9. An interference of H3K9 dimethylation by SUVR4 occurs by a pre-existing phosphorylation at S10. Hence, cross-talk in plants exists between phosphorylation of H3S10 and methylation, acetylation or phosphorylation of neighbouring amino acid residues. AtAurora1 undergoes autophosphorylation in vivo regardless of the presence of substrate, and forms dimers in planta . Of the three ATP-competitive Aurora inhibitors tested, Hesperadin was most effective in reducing the in vivo kinase activity of AtAurora1. Hesperadin consistently inhibited histone H3S10 phosphorylation during mitosis in Arabidopsis cells, but did not affect other H3 post-translational modifications, suggesting a specific inhibition of AtAurora in vivo . Inactivation of AtAurora also caused lagging chromosomes in a number of anaphase cells, but, unlike the situation in mammalian cells, Hesperadin did not influence the microtubule dynamics in dividing cells. 相似文献
994.
Guido Achermann Theresa M. Ballard Francesca Blasco Pierre-Emmanuel Broutin Bernd Büttelmann Holger Fischer Martin Graf Maria-Clemencia Hernandez Peter Hilty Frédéric Knoflach Andreas Koblet Henner Knust Anke Kurt James R. Martin Raffaello Masciadri Richard H.P. Porter Heinz Stadler Andrew W. Thomas Gerhard Trube Jürgen Wichmann 《Bioorganic & medicinal chemistry letters》2009,19(19):5746-5752
Through iterative design cycles we have discovered a number of novel new classes where the imidazo[1,5-a][1,2,4]-triazolo[1,5-d][1,4]benzodiazepine was deemed the most promising GABAA α5 inverse agonist class with potential for cognitive enhancement. This class combines a modest subtype binding selectivity with inverse agonism and has the most favourable molecular properties for further lead optimisation towards a central nervous system (CNS) acting medicine. 相似文献
995.
996.
Joseph K. Bailey Jennifer A. Schweitzer Francisco úbeda Julia Koricheva Carri J. LeRoy Michael D. Madritch Brian J. Rehill Randy K. Bangert Dylan G. Fischer Gerard J. Allan Thomas G. Whitham 《Philosophical transactions of the Royal Society of London. Series B, Biological sciences》2009,364(1523):1607-1616
Using two genetic approaches and seven different plant systems, we present findings from a meta-analysis examining the strength of the effects of plant genetic introgression and genotypic diversity across individual, community and ecosystem levels with the goal of synthesizing the patterns to date. We found that (i) the strength of plant genetic effects can be quite high; however, the overall strength of genetic effects on most response variables declined as the levels of organization increased. (ii) Plant genetic effects varied such that introgression had a greater impact on individual phenotypes than extended effects on arthropods or microbes/fungi. By contrast, the greatest effects of genotypic diversity were on arthropods. (iii) Plant genetic effects were greater on above-ground versus below-ground processes, but there was no difference between terrestrial and aquatic environments. (iv) The strength of the effects of intraspecific genotypic diversity tended to be weaker than interspecific genetic introgression. (v) Although genetic effects generally decline across levels of organization, in some cases they do not, suggesting that specific organisms and/or processes may respond more than others to underlying genetic variation. Because patterns in the overall impacts of introgression and genotypic diversity were generally consistent across diverse study systems and consistent with theoretical expectations, these results provide generality for understanding the extended consequences of plant genetic variation across levels of organization, with evolutionary implications. 相似文献
997.
Kiranmai Durvasula Kaemwich Jantama Kyle Fischer Adrian Vega Ben Koopman Spyros A. Svoronos 《Biotechnology progress》2009,25(4):973-979
Paracoccus pantotrophus expresses two nitrate reductases—membrane bound nitrate reductase (Nar) and periplasmic nitrate reductase (Nap). In growth experiments with two denitrifying species (Paracoccus pantotrophus and Alcaligenes eutrophus) that have both Nap and Nar and two species (Pseudomonas denitrificans and Pseudomonas fluorescens) with Nar only, it was found that diauxic lag is shorter for bacteria that express Nap. In P. pantotrophus, napEDABC encodes the periplasmic nitrate reductase. To analyze the effect of Nap on diauxic lag, the nap operon was deleted from P. pantotrophus. The growth experiments with nap? mutant resulted in increased diauxic lag when switched from aerobic to anoxic respiration, suggesting Nap is responsible for shorter lags and helps in adaptation to anoxic metabolism after transition from aerobic conditions. © 2009 American Institute of Chemical Engineers Biotechnol. Prog., 2009 相似文献
998.
Bjoern Sill Ivan V. Alpatov Christina A. Pacak Douglas B. Cowan 《Journal of visualized experiments : JoVE》2009,(28)
Rodent surgery is often an important component in assessing the utility of engineered tissues. A wide variety of surgical procedures can be performed in common laboratory rats or mice and these quite frequently serve as an intermediate step between bench-top experiments and large animal testing or human trials. Given that rodents provide an established, cost-effective, and physiologically-relevant model system in which to test novel combinations of scaffolding materials and cells, they are particularly well-suited for cardiovascular tissue engineering studies. Presently, we describe an open-heart surgical procedure to implant engineered tissue containing myogenic progenitor cells in the atrioventricular (AV) groove of a rat heart. These implants are intended to create an electrical conduit between the right atrium and right ventricle with the ultimate goal of providing an alternative treatment to conventional pacemaker implantation in pediatric patients with complete heart block[1]. The engineered tissue is implanted in the AV-groove by means of a thoracotomy. For our purposes, Lewis rats are anesthetized and invasively ventilated to maintain positive airway pressure during the sterile surgical procedure. The approach to the heart is performed by a right thoracotomy through an antero-lateral incision at the 5th intercostal space. The tissue construct is fixed in the AV groove using a single 7-0 Prolene suture and positioned between the right ventricle and atrium at the ventral portion of the heart. The epicardium is partially removed to allow direct contact between the recipient myocardial cells and those contained in the engineered tissue. Following implantation, the chest wall is closed in layers, any pneumothorax is evacuated, and the animal is extubated and treated with analgesic.Download video file.(95M, mp4) 相似文献
999.
1000.
Ilka Hoof Bjoern Peters John Sidney Lasse Eggers Pedersen Alessandro Sette Ole Lund Søren Buus Morten Nielsen 《Immunogenetics》2009,61(1):1-13
Binding of peptides to major histocompatibility complex (MHC) molecules is the single most selective step in the recognition
of pathogens by the cellular immune system. The human MHC genomic region (called HLA) is extremely polymorphic comprising
several thousand alleles, each encoding a distinct MHC molecule. The potentially unique specificity of the majority of HLA
alleles that have been identified to date remains uncharacterized. Likewise, only a limited number of chimpanzee and rhesus
macaque MHC class I molecules have been characterized experimentally. Here, we present NetMHCpan-2.0, a method that generates quantitative predictions of the affinity of any peptide–MHC class I interaction. NetMHCpan-2.0 has been trained on the hitherto largest set of quantitative MHC binding data available, covering HLA-A and HLA-B, as well
as chimpanzee, rhesus macaque, gorilla, and mouse MHC class I molecules. We show that the NetMHCpan-2.0 method can accurately predict binding to uncharacterized HLA molecules, including HLA-C and HLA-G. Moreover, NetMHCpan-2.0 is demonstrated to accurately predict peptide binding to chimpanzee and macaque MHC class I molecules. The power of NetMHCpan-2.0 to guide immunologists in interpreting cellular immune responses in large out-bred populations is demonstrated. Further,
we used NetMHCpan-2.0 to predict potential binding peptides for the pig MHC class I molecule SLA-1*0401. Ninety-three percent of the predicted
peptides were demonstrated to bind stronger than 500 nM. The high performance of NetMHCpan-2.0 for non-human primates documents the method’s ability to provide broad allelic coverage also beyond human MHC molecules.
The method is available at .
Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users. 相似文献