125,157 research outputs found
Going Beyond Counting First Authors in Author Co-citation Analysis
No full textThe present study examines one of the fundamental aspects of author co-citation analysis (ACA) - the way co-citation
counts are defined. Co-citation counting provides the data on which all subsequent statistical analyses and mappings
are based, and we compare ACA results based on two different types of co-citation counting - the traditional type that
only counts the first one among a cited work's authors on the one hand and a non-traditional type that takes into
account the first 5 authors of a cited work on the other hand. Results indicate that the picture produced through this non-traditional author co-citation counting contains more coherent author groups and is therefore considerably clearer. However, this picture represents fewer specialties in the research field being studied than that produced through the traditional first-author co-citation counting when the same number of top-ranked authors is selected and analyzed. Reasons for these effects are discussed
Dispelling the Myths Behind First-author Citation Counts
No full textWe conducted a full-scale evaluative citation analysis study of scholars in the XML research field to explore just how different from each other author rankings resulting from different citation counting methods actually are, and to demonstrate the capability of emerging data and tools on the Web in supporting more realistic citation counting methods. Our results contest some common arguments for the continued
use of first-author citation counts in the evaluation of scholars, such as high correlations between author rankings by first-author citation counts and other citation
counting methods, and high costs of using more realistic citation counting methods that are not well-supported by the ISI databases. It is argued that increasingly available digital full text research papers make it possible for citation analysis studies to go beyond what the ISI databases have directly supported and to employ more
sophisticated methods
Deformation of the Calabrian Arc subduction complex and its relation to STEP activity at depth
No full textThe interplay between a Phytophthora RXLR effector and an Arabidopsis lectin receptor kinase
No full textPhytophthora infestans – the causal agent of potato late blight – secretes a plethora of effector proteins to facilitate plant infection. The central subject of this thesis is ipiO, one of the first cloned Phytophthora genes with a putative function in pathogenicity as was anticipated based on its in planta induced (ipi) expression, in particular during early stages of host infection. IPI-O contains two striking motifs: RXLR-dEER and RGD. RGD is a cell adhesion motif and was shown to be involved in binding to the extracellular lectin domain of LecRK-I.9, a lectin receptor kinase of Arabidopsis. The RXLR-dEER motif plays a role in effector trafficking into host cells and is shared by several secreted oomycete effector proteins which are known to function as race-specific avirulence (Avr) factors. In a previous study, that was aimed at identifying novel pairs of P. infestans Avr and host plant resistance (R) genes, a high-throughput effector genomics screen identified ipiO as Avr-blb1, the counterpart of the late blight R gene Rpi-blb1 which originates from the nightshade Solanum bulbocastanum. Often R genes exploited in late blight resistance breeding become rapidly ineffective as a result of adaptation of P. infestans. However, unlike most late blight R genes that interact in a gene-for-gene manner with Avr genes, Rpi-blb1 seemed to have the potential to remain its effectiveness. In section 2 we monitored the genetic variation and distribution of the ipiO family in an extensive isolate collection of P. infestans and closely related species. This resulted in the identification of 16 IPI-O variants that could be sub-divided in three distinct classes. Variants from class I and class II were shown to induce cell death when co-infiltrated with Rpi-blb1 in Nicotiana benthamiana. Class III consists solely of the highly divergent variant IPI-O4, that is not able to trigger Rpi-blb1-mediated cell death. Class I is highly diverse and represented in all P. infestans isolates analyzed so far, except in two Mexican P. infestans isolates. The latter two are capable to infect Rpi-blb1 plants, suggesting that the lack of class I variants in the genome of these strains allows them to escape recognition by Rpi-blb1 plants. We propose that profiling of the ipiO variants within P. infestans populations can predict the effectiveness of Rpi-blb1-mediated resistance in potato and, as such, can facilitate integrated disease management. Section 3 of this thesis deals with legume-like lectin receptor kinases (LecRKs), membrane-spanning proteins with potential roles in adaptive responses and cell wall integrity. We present an inventory and a phylogenetic analysis of the Arabidopsis LecRK gene family. The rationale behind this study was to gain better insight into the diversity of LecRKs and their potential roles in plant defense. A comprehensive expression analysis based on exploration of existing databases revealed that several LecRK genes are induced upon treatment with elicitors or during pathogen infection. Based on the phylogenetic analysis we have reclassified the LecRK genes and proposed a new nomenclature. LecRK-I.9, one of the clade I Arabidopsis LecRKs which binds the RGD cell adhesion motif of IPI-O, was shown to mediate adhesion between the cell wall (CW) and plasma membrane (PM). In contrast, IPI-O disrupts these adhesions by virtue of its RGD motif. We analyzed Arabidopsis LecRK-I.9 knock-out lines (lecrk-I.9) for their response to pathogen infection, in particular to Phytophthora brassicae. We also analyzed transgenic Arabidopsis lines expressing ipiO, and observed that both the ipiO-expressing lines and lecrk-I.9 lines are impaired in their resistance to oomycete pathogens. To unravel the mechanisms underlying this phenomenon we analysed callose deposition upon MAMP (i.e. flg22) treatment and investigated the strength of CW-PM adhesions under plasmolysis-inducing conditions. The results indicated that LecRK-I.9 is not only important for the maintenance of the CW-PM continuum, but also in MAMP-triggered immunity. Also here, both the ipiO-expressing lines and the lecrk-I.9 knock-outs displayed a destabilized CW-PM continuum and impaired callose deposition, and hence, they can be regarded as phenocopies. Arabidopsis plants that constitutively express LecRK-I.9 were smaller in size, and displayed increased levels of anthocyanin and lignin. Additionally, these lines were shown to exhibit enhanced resistance to P. brassicae. Furthermore, we studied transgenic potatoes that constitutively Arabidopsis LecRK-I.9. In comparison to the parental control potato line the transgenic lines were less susceptible to mild and moderately aggressive P. infestans isolates, but the increased tolerance was not sufficient to provide resistance to aggressive isolates. These results strongly suggest that LecRK-I.9 is a novel resistance component that plays a role in defense against Phytophthora. In Section 4 we describe a novel method for propagating P. brassicae zoospores on an intermediate host plant. This resulted in the production of high numbers of zoospores thereby facilitating highly reproducible small and large scale inoculation experiments. This thesis is completed with a general discussion (Section 5) addressing the current understanding of effector uptake by host cells, the subsequent recognition by cognate R proteins mediating effector-triggered immunity, and RXLR-dEER effector diversity. We also discuss the role of the RGD motif in effectors of both animal and plant pathogens, and the potential functions of LecRKs. Finally, we high-light the advantages of Arabidopsis-Phytophthora pathosystems as research object. <br/
Pragmatic Case Studies as a Source of Unity in Applied Psychology
No full textTo unify or not to unify applied psychology: that is the question. In this article we review pendulum swings in the historical efforts to answer this question—from a comprehensive, positivist, “top-down,” deductive yes between the 1930s and the early 60s, to a postmodern no since then. A rationale and proposal for a limited, “bottom-up,” inductive yes in applied psychology is then presented, employing a case-based paradigm that integrates both positivist and postmodern themes and components. This paradigm is labeled “pragmatic psychology” and, its specific use of case studies, the “Pragmatic Case Study Method” (“PCS Method”). We call for the creation of peer-reviewed journal-databases of pragmatic case studies as a foundational source of unifying applied knowledge in our discipline. As one example, the potential of the PCS Method for unifying different angles of theoretical regard is illustrated in an area of applied psychology, psychotherapy, via the case of Mrs. B. The article then turns to the broader historical and epistemological arguments for the unifying nature of the PCS Method in both applied and basic psychology.Peer reviewe
Dr. Edwin Wright Collection: Author Unknown
No full textNotes - The author relates several short stories about his neighbours including Alex McDonell, homesteading and life around Meanook and Athabasca (1 page
Appropriate Similarity Measures for Author Cocitation Analysis
No full textWe provide a number of new insights into the methodological discussion about author cocitation analysis. We first argue that the use of the Pearson correlation for measuring the similarity between authors’ cocitation profiles is not very satisfactory. We then discuss what kind of similarity measures may be used as an alternative to the Pearson correlation. We consider three similarity measures in particular. One is the well-known cosine. The other two similarity measures have not been used before in the bibliometric literature. Finally, we show by means of an example that our findings have a high practical relevance.information science;Pearson correlation;cosine;similarity measure;author cocitation analysis
Measurement of the ratio of branching fractions B(B0→K∗0γ )/B(B0s→φγ ) and the directCP asymmetry inB 0→K∗0γ
No full textThe ratio of branching fractions of the radiative B decays B0→K⁎0γ and B0s→ϕγ has been measured using an integrated luminosity of 1.0 fb−1 of pp collision data collected by the LHCb experiment at a centre-of-mass energy of s√=7TeV. The value obtained is
B(B0→K⁎0γ)B(B0s→ϕγ)=1.23±0.06(stat.)±0.04(syst.)±0.10(fs/fd),
where the first uncertainty is statistical, the second is the experimental systematic uncertainty and the third is associated with the ratio of fragmentation fractions fs/fd. Using the world average value for B(B0→K⁎0γ), the branching fraction B(B0s→ϕγ) is measured to be (3.5±0.4)×10−5.
The direct CP asymmetry in B0→K⁎0γ decays has also been measured with the same data and found to be
ACP(B0→K⁎0γ)=(0.8±1.7(stat.)±0.9(syst.))%.
Both measurements are the most precise to date and are in agreement with the previous experimental results and theoretical expectations
The construction of Karen Karnak: The multi-author-function
No full textThis thesis is situated within the comparatively recent developments of Web 2.0 and the emergence of interactive WikiMedia, and explores the mode of authorship within a Read/Write culture compared to that of a Read/Only tradition. The hypothesis of this study is that the role of the audience has become merged with the author, and as such, represents new functions and attributes, distinct from a more conventional concept of authorship, in which the roles of audience and author are more separate. Read/Write and participatory culture, as defined by this study, is focused on collaboration, and includes the influences of D.I.Y. culture, Open-Source practices and the production of text by multiple authors. Multi-authorship presents a re-thinking of several concepts which support the notion of the individual author, since the focus of multi-authorship is not on attribution and ownership of a finished text, but on the continued malleability of a text. Modes of multi-authorship, demonstrated in the use of the pseudonyms Alan Smithee and Karen Eliot, represent declarative authors whose names signify multiple origins, whilst concurrently indicating a distinct body of work. The function of these names form an important context to this study, since primary research involves the construction of an experimental mode of multi-authorship utilising WikiMedia technology and the interaction of thirty nine participants, who are invited to create a body of work under the collective pseudonym Karen Karnak. The data generated by this experiment is analysed using aspects of Michel Foucault's author-function to identify and determine power structures inherent in the WikiMedia context. The interplay of power structures, including concepts such as identity, ownership and the body of work, affect the resulting mode of authorship and contribute to the construction of Karen Karnak, suggesting further areas of research into the emerging multi-author
The Phytophthora infestans avirulence gene PiaAvr4 and its potato counterpart R4
No full textThe potato late blight disease that is caused by the oomycete pathogen Phytophthora infestans is a major threat for potato crops worldwide. In recent years research on oomycete plant pathogens was boosted by the availability of novel genomic tools and resources for several oomycete genera, such as Phytophthora, Hyaloperonospora, Pythium and Aphanomyces. This has led to the identification of genes involved in diverse biological processes such as sporulation, mating, signaling and pathogenesis. One of the approaches that breeders use to obtain late blight resistant potato cultivars is the introgression of resistance traits from wild Solanum species into the cultivated potato Solanum tuberosum. The pathogen, however, is able to circumvent this resistance; it is often lost shortly after introduction of new cultivars. To better understand the mechanisms underlying this loss of resistance it is of utmost importance to gain insight into the characteristics of the cognate avirulence (Avr) genes of the pathogen. According to the gene-for-gene model Avr genes encode effectors that trigger resistance responses mediated by resistance (R) genes. This thesis first describes the identification of a P. infestans Avr gene, in particular the elicitor activity of the encoded effector protein, the domain structure of the effector and its putative sub-cellular localization. In the second part the recognition specificity of the corresponding R gene and the identification of a marker linked to this R gene are described. Chapter 1 summarizes the advances in oomycete genomics in recent years and the tremendous progress that has been made in gene discovery in oomycete plant pathogens. It describes the different oomycete species that have been studied in more detail and assesses which species are suitable model species for research on oomycete-plant interactions. The identification of the P. infestans avirulence gene PiAvr4 is presented in Chapter 2. PiAvr4, which encodes an RXLR-dEER effector protein, was isolated by positional cloning. AFLP markers were used for landing on BACs and cDNA-AFLP markers pinpointed the gene of interest. Transformation of race 4 strains with PiAvr4 resulted in transformants that are avirulent on the R4 differential of the Mastenbroek differential set (clone Ma-R4). Moreover, in planta expression of PiAvr4 resulted in a necrotic response on clone Ma-R4 but not on plants lacking R4 such as Bintje. All together this proves that PiAvr4 is the avirulence gene that corresponds to the R gene present in clone Ma-R4. In many identified avirulence proteins one or a few amino acid changes in the protein abolish avirulence function. In case of PiAvr4, race 4 strains have frame shift mutations in the open reading frame, resulting in a truncated protein that is not functional as avirulence factor. Effectors within the RXLR-dEER family are rapidly evolving. The selective pressure is targeted predominantly on the C-terminal region of these proteins. Despite this selective pressure the majority of these proteins carry motifs that can be distinguished using Hidden Markov Models searches. They are named W, Y and L motifs after the conserved tryptophan (W), tyrosine (Y) and leucine (L) residues, respectively. As described in Chapter 3 PiAvr4 carries three W motifs and a single Y motif. The motifs together with their flanking regions were tested for activity on Ma-R4 plants. Agroinfection of constructs carrying the W2 motif in combination with either the W1 or W3 motif resulted in a necrotic response. Moreover, we showed that the PiAvr4 homolog PmirAvh4, isolated from Phytophthora mirabilis was also able to elicit a necrotic response on the Ma-R4 potato clone. For several Phytophthora RXLR-dEER effectors it was demonstrated that these proteins are targeted into the host cell and that the RXLR-dEER motif is required for translocation. In Chapter 4 we investigated whether PiAvr4 and IPI-O, like other RXLR-dEER effectors, are also targeted into the host cell. A race 4 P. infestans isolate was transformed with constructs encoding either PiAvr4 or IPI-O fused to a monomeric red fluorescent protein (mRFP) at the C-terminus. Fluorescence microscopy of these transformants showed no specific mRFP fluorescence in free living, non-sporulating mycelium. However, in germinating cysts, the tips of germ tubes and appressoria showed mRFP fluorescence, and during infection of etiolated potato plantlets localized fluorescence was visible at the haustorial neck. Haustoria are highly specialized infection and feeding structures that are in close contact with the plant cell and have a putative role in delivering effector proteins into the host cell. In order to monitor the development of the infection a novel experimental set-up was developed. In this method etiolated in vitro grown potato plantlets are inoculated with P. infestans, which has the advantage that there is no autofluorescence of chlorophyll that masks the mRFP fluorescence and thus disturbs the microscopic analysis in green plant tissues. The lack of chlorophyll does not seem to interfere with infection; zoospores are capable to encyst and to germinate, and the etiolated tissues are readily colonized by P. infestans. The recognition specificity of R4 potato differentials is described in Chapter 5. Initially two different potato clones were developed as R4 differentials; The Mastenbroek differential set, developed in the Netherlands, contains the clone Cebeco44-31-5 (designated as Ma-R4) and the Black differential set, developed in Scotland, contains clone 1563 c (14) (designated as Bl-R4). Virulence assays using several wild type P. infestans strains revealed that the Bl-R4 clone is susceptible to all isolates that are avirulent on clone Ma-R4. Only one single isolate was found to be avirulent on clone Bl-R4, but virulent on Ma-R4. Moreover, in transient expression assays with binary PVX constructs carrying PiAvr4, the Ma-R4 clone but not the Bl-R4 clone responded with an HR. Similar to the R3 locus two different recognition specificities seem to exist for R4. The R3a and R3b genes are located on one locus but whether this is the case for the two R4 genes (named R4Ma and R4Bl, respectively) remains to be determined. Resistance to P. infestans strains carrying PiAvr4 segregates in an 1:1 ratio in two independent potato F1 populations suggesting that R4Ma resistance is determined by a single dominant locus. More in depth studies on the recognition of PiAvr4 by its cognate R protein are hampered by the fact that the resistance gene R4Ma has not yet been identified. In Chapter 6 nucleotide binding site (NBS) profiling was used to generate R4Ma-associated markers. NBS profiling is a biased approach based on PCR amplification of conserved NBS motifs in R genes and R gene homologs. In a bulked segregant analysis, DNA of resistant and susceptible F1 progeny was pooled and used as template for NBS profiling. Several candidate markers were found but eventually one amplified fragment was found to co-segregate with resistance mediated by R4Ma. DNA sequencing of this fragment revealed high similarity to BAC sequences that are mapped to potato chromosome 12. Moreover, the R4Ma marker is homologous to members of the Rx/Gpa2 gene family. Chapter 7 focuses on the secreted effectors of plant pathogenic oomycetes, with special attention to RXLR-dEER effectors, and the role of these proteins in pathogenesis. The RXLR-dEER effector family is rapidly evolving and comprises all secreted oomycete avirulence proteins that are identified up till now. There is now ample evidence that oomycetes utilize the RXLR-dEER domain to deposit effectors inside host cells. Furthermore, this chapter discusses the experimental results described in this thesis in the light of present knowledge on gene-for-gene interactions, effector recognition and late blight resistance. <br/
- …
