98,822 research outputs found
Joshua Davis: Author of Spare Parts
No full textCitation: K-State First (2016). Joshua Davis: Author of Spare Parts [Flier]. Manhattan, Kansas: K-State First.Flyer advertising Joshua Davis's author talk at Kansas State University
Steven Johnson Author Talk Poster
No full textK-State Book NetworkA poster advertising an author talk by Steven Johnson at Kansas State University on September 3, 2014. Steven Johnson's book "The Ghost Map" was the 2014-2015 common book
Four distinct leadership roles in sport (as defined by Fransen, Vanbeselaere, et al., 2014).
No full textFour distinct leadership roles in sport (as defined by Fransen, Vanbeselaere, et al., 2014).</p
A new stygobiont species of Halocaridinides Fujino & Shokita, 1975 (Crustacea, Decapoda, Caridea, Atyidae) from caves on Socotra Island (Yemen), with notes on the genus
No full textFransen, Charles H.J.M., Damme, K. Van (2018): A new stygobiont species of Halocaridinides Fujino & Shokita, 1975 (Crustacea, Decapoda, Caridea, Atyidae) from caves on Socotra Island (Yemen), with notes on the genus. Zootaxa 4442 (2): 241-261, DOI: 10.11646/zootaxa.4442.2.
An Anthology of Early British Motorcycle Travel Literature
No full textCollaborative book project in association with the International Journal of Motorcycle Studies (IJMS) and Riders for Health.
Along with a foreword by Steven E. Alford and Suzanne Ferriss, this volume contains three early twentieth-century British motorcycle travel narratives : Captain W. H. L. Watson’s Adventures of a Despatch Rider (1915), Lady Warren’s Through Algeria & Tunisia on a Motor-bicycle (1922) and C. K. Shepherd’s Across America by Motor-Cycle (1922). Interactive colour maps are available at :
Additionally, this publication follows a social enterprise model employed in a previous motorcycle travel project entitled Essex-Dakar with all profits helping support notable causes, in this case, Riders for Health.
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Book Review : Goodmann, T. (2009) The Road Worst Traveled. International Journal of Motorcycle Studies. [Internet]. vol.5, Issue 2: Fall. Available at : <http://ijms.nova.edu/Fall2009/IJMS_Rvw.Goodmann.html
Publication : Bart Fransen et Cyriel Stroo, "The Ghent Altarpiece. Research and Conservation of the Exterior", Bruxelles, Institut du Patrimoine artistique, 2020
No full textThe Ghent Altarpiece. Research and Conservation of the Exterior Sous la direction de Bart Fransen and Cyriel Stroo Avec les contributions de A.-S. Augustyniak, Chr. Ceulemans, A. Coudray, D. Deneffe, L. Depuydt, B. Devolder, H. Dubois, B. Fransen, A. Genbrugge, J.-A. Glatigny, K. Janssens, S. Jones, J. Ketels, L. Mortiaux, N. Laquière, M. Martens, Cl. Mehagnoul, M. Postec, J. Reyniers, Fr. Rosier, J. Sanyova, M. H. Smith, R. Spronk, Gr. Steyaert, C. Stroo, P. Vandenabeele, G. Vandersnickt, A...
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
Nippontonia christellae Fransen, 2013, spec. nov.
No full textNippontonia christellae spec. nov. (figs 1–9) Material examined. 1 ovigerous female holotype (pocl. 4.75 mm), RMNH.CRUS.D. 53861; 1 male paratype (pocl. 3.80 mm), RMNH.CRUS.D. 53837; 1 ovigerous female paratype (pocl. 4.81 mm), RMNH.CRUS.D. 53841: stn. SEM. 18: Malaysia, Sabah, Semporna area, Ligitan Island, Ligitan 4, 04014'06.5"N 118048 '26,5"E; 4.xii. 2010; 15 m depth; in the sponge Acanthostrongylophora ingens (Thiele, 1899) (id. N.J. de Voogd); collected by C.H.J.M. Fransen; photo 533, 540 – 552. Material for comparison. Nippontonia minirostris Bruce & Bauer, 1997. 1 paratype non-ovigerous female (pocl. 2.4 mm), RMNH.CRUS.D. 47746; Stn YMP- 1231, Japan, Ryukyu Is., Kerama group, Aka-jima, Nishihama; 22.iv. 1994; depth 15 m; in unidentified black sponge; collected by K. Nomura. 2 ovigerous females (pocl. 2.6, 2.7, and 2.8 mm), 2 males (pocl. 2.2 and 3.0 mm), and 1 juvenile (pocl. 1.8 mm), OUMNH 2010 -02-0056; 1 ovigerous female (pocl 2.4 mm), RMNH.CRUS.D. 54442: Taiwan, Green Island, General Rock, 22 º 40.567 ’N 121 º 23.618 ’E; from big black sponge; depth 10–15 m; 21.vii. 2009; leg. T. Naruse TAI 0 24. Description. Medium-sized shrimp (fig. 1) with subcylindrical, oblong body shape. Carapace smooth (fig. 1), glabrous. Rostrum (figs. 1, 2A, B) very short, not reaching beyond eyes, laterally compressed, triangular in dorsal view, with one small dorsal obtuse tooth, unarmed ventrally, lateral carina not developed. Supra-orbital, epigastric, and hepatic teeth absent. Minute antennal tooth present or absent. Orbit obsolescent. Inferior orbital angle (fig. 2 A) slightly produced, broadly rounded in dorsal view. Pterygostomial angle (fig. 2 A) strongly produced, rounded. Abdominal segments (fig. 1) smooth. Third segment not produced posterodorsally. Pleura all broadly rounded. Sixth segment as long as fifth, posteroventral angle feebly produced, posterolateral angle feebly acute. Telson (fig. 2 C) 1.5 times as long as sixth abdominal segment and 1.6 times longer than anterior width; lateral margins slightly converge posteriorly; two pairs of large sized submarginal dorsal spines present at 0.1 and 0.4 of telson length; posterior margin broadly rounded, about 0.66 of anterior width, with three pairs of spines. Lateral spines short, about third of dorsal spines. Intermediate spines well developed, about twice as long as lateral spines, 1.3 times length of submedian spines. Eyes (fig. 2 A, B) well developed. Large cornea globular, obliquely set on stalks, without accessory pigment spot. Eyestalks more than twice as long as proximal width, not swollen proximally in dorsal view. Antennular peduncle (fig. 2 D) slender, about twice as long as eyes. Proximal segment long, slender, 3.6 times longer than wide; stylocerite slender, acute, reaching to third of segment; lateral margin slightly convex, anterolateral margin not produced, with one strong distolateral tooth, distodorsal margin with distinct protrusion with row of setae; medial ventral margin with small but distinct acute tooth at mid length of segment. Statocyst normally developed, without statolith. Intermediate and distal segments short, together equal to 0.34 of proximal segment length. Upper flagellum biramous, with the first 7–8 segments fused. Shorter free ramus uni-segmented, longer free ramus with about 10 segments. Aesthetascs present in distal part of fused rami and uni-segmented short free ramus. The lower flagellum slender, about as long as the longer free ramus of the upper flagellum. Antennal basicerite (fig. 2 E) without lateral tooth. Ischiocerite and merocerite normal. Carpocerite slender, almost reaching to mid length of scaphocerite. Scaphocerite long, slender, with lamella strongly reduced, without setae. Lateral border slightly convex, ending in a very long robust acute distolateral tooth. Thoracic sternites very narrow, unarmed. Mandible (fig. 3 A, B) with cylindrical slender, strongly reduced molar process without any armature, distally two-segmented; incisor process distally expanded with row of about 20 posteromedial teeth; without palp. Maxillula (fig. 3 C) with bilobed palp; upper lacinia broad, furnished with several rows of stout simple and serrulate setae along median margin; lower lacinia short with long serrulate setae distally. Maxilla (fig. 3 D) with stout simple palp with one proximal seta. Basal endite well developed, not bilobed, broad with about 18 simple setae along anterior and medial margins. Coxal endite not developed, median region slightly convex. Scaphognathite as usual for the genus. First maxilliped (fig. 4 A) with simple non-setose palp. Basal endite well developed, subrectangular, distinctly separated from coxal endite, fringed medially with fine setulose and simple setae. Coxal endite convex with fine setulose and simple setae medially. Caridean lobe distinct but not well developed, with plumose marginal setae. Flagellum of exopod short with few lateral and distal plumose setae. Epipod well developed, indistinctly bilobed. Second maxilliped (fig. 4 B) with rectangular dactylar segment, about 4 times longer than wide, slightly convex medially, bearing row of stout biserrulate spines. Propodal segment longer than dactylar segment, with rounded distomedial angle with long serrulate setae in medial half. Carpus short and merus normal. Ischium completely fused to basis. Basis with long exopod with plumose setae in distal fifth. Coxa slightly produced medially, with oblong epipod laterally. Third maxilliped (fig. 4 C) with moderately broad antepenultimate segment, about 3 times longer than proximal width. Basis completely fused with ischiomerus. Medial margin with simple setae. Penultimate segment slender, 3.8 times longer than wide, 0.39 of length of antepenultimate segment, with rows of long, robust setulose setae on medial border. Terminal segment 3.0 times longer than wide, almost half length of penultimate segment, with long, robust serrulate and simple setae medially and distally. Exopod long, just overreaching distal margin of antepenultimate segment; with long plumose setae in distal third. Coxa not produced medially, lateral plate well developed, convex; oblong epipod laterally. Without arthrobranch. First pereiopod (fig. 4 D) moderately robust, overreaching scaphocerite by chela. Chela with palm subcylindrical, slightly bowed, about twice as longer as wide. Fingers (fig. 4 E) 0.8 of palm length, subspatulate, with brushes of setae. Cutting edges poorly developed, entire. Tip of dactylus and fixed finger tridentate, central tooth robust, articulate. Cleaning setae present proximally on palm and distoventral end of carpus. Carpus 1.4 times length of chela, 5.0 times longer than wide. Merus about as long as carpus, 1.4 times as long as ischium. Basis normal. Coxa with medial setose process. Second pereiopods (fig. 5) large, symmetrical in shape, unequal in size. Major cheliped (fig. 5 A) with ischium 0.64 times length of merus, distally armed with few small acute tubercles. Merus as long as carpus, 2.5 times longer than central depth, with minute, acute tubercles along medial margin. Carpus 0.66 of palm length, strongly excavate dorsally. Palm subcylindrical, somewhat compressed, unarmed, strongly swollen posteriorly, 1.5 times longer than proximal depth. Fingers (fig. 5 B, C) 0.62 of palm length, cutting edges entire, tips strongly hooked, with several brushes of setae. Minor cheliped (fig. 5 D) as major cheliped. Fingers of chela (fig. 5 E) as long as palm. Dactylus slender, with medial longitudinal carina, tip strongly hooked, distal 2 / 5 th of cutting edge entire, proximal 3 / 5 th with minutely tuberculate surface. Fixed finger oblong triangular with distal fifth of cutting edge entire, proximal 4 / 5 th of cutting edge with minutely tuberculate surface, tip strongly hooked. The ambulatory pereiopods (fig. 6) relatively robust, similar. Third pereiopod (fig. 6 A) reaching with dactylus to distal margin of antennular peduncle. Dactylus (fig. 6 B, C) short, about twice as long as proximal depth, strongly recurved, slightly compressed, uniformly tapering, with distinct slender unguis; with row of 4–6 obtuse teeth in middle part of flexor margin, distalmost tooth largest, corpus without setae. Propodus about five times longer than wide, about 6.5 times length of dactylus, with row of 6–9 ventral spines including distoventral one. Carpus, merus and ischium 0.87, 1.4 and 0.82 of propodus length, unarmed. Fourth pereiopod (fig. 6 D) propodus with 7–9 spines along ventral margin, dactylus (fig. 6 E, F) with row of 4–6 obtuse teeth in middle of flexor margin of corpus. Fifth pereiopod (fig. 6 G) propodus with two distoventral spines, distoventral cleaning brush not developed, dactylus (fig. 6 H, I) with one obtuse tooth in middle of flexor margin of corpus. Female first pleopod (fig. 7 A) with exopod more than twice length of endopod. Second pleopod with normal appendix interna. Male first pleopod (fig. 7 B) with exopod twice as long as endopod. Endopod (fig. 7 C) with row of simple short setae medially, long serrulate setae distally and plumose setae laterally. Male second pleopod (fig. 7 D) with corpus of appendix masculina (fig. 7 E) not developed, with two long strongly serrulate setae extending beyond normal appendix interna. Uropods (fig. 2 C) extending beyond tip of telson. Protopodite unarmed laterally. Exopod with lateral border with 9–11 strong teeth, increasing in size distally. Very large mobile spine present distolaterally, about 1.8 times longer than dorsal telson spines. Eggs 0.6 mm in diameter. Colouration. Generally dotted with brown to dark green chromatophores over body and appendages (figs. 8, 9). Eyestalks with longitudinal broad brown-green bands. Chelipeds with brown-green reticulate pattern or large dots. Hepatopancreas dark brown to black. Eggs without pigment spot bright orange (fig. 9 upper), with spots brownish (fig. 9 lower). Etymology. The species is named after the author’s sister-in-law, Christel van Eijnatten, with respect and admiration for her inspiring perseverance and positivism in conquering life again after it was almost taken from her. The specific name christellae is a noun in the genitive singular. Host. Acanthostrongylophora ingens (Thiele, 1899) (Porifera: Petrosiidae: Haplosclerida) (fig. 8), identified by N.J. de Voogd. The type species of the genus has been collected from an unidentified black sponge. Distribution. The species is only know from its type locality: Ligitan Island, Semporna area, Sabah, Malaysia. Systematic position Morphological data. The present three specimens differ from N. minirostris in the following characters: 1) the specimens are about twice as large in size as the 9 specimens from the type series as well as the material from Taiwan of N. minirostris; 2) the scaphocerite is almost three times as long as the eye while slightly longer than the eye in N. minirostris; 3) the proximal segment of the antennular peduncle is distinctly longer than the eye while falling short of the eye in the types of N. minirostris and falling short to slightly overreching the eye in the Taiwan material; 4) the outer flagellum of the antennula has the proximal 7–8 segments fused while the proximal 3–6 in N. minirostris; 5) the reduced molar process of the mandible is 2 -segmented while unsegmented in the N. minirostris holotype; 6) the flexor margin of the dactylus of the third pereiopod has a row of 4–6 obtuse teeth in the middle part of the flexor margin of which the distalmost tooth is the largest while one or two acute teeth are present in N. minirostris. The rostrum of the holotype of N. minirostris was depicted in being short and obtuse but without an indication of a subdistal tooth. A subdistal obtuse tooth like in the new species has been observed though in the paratype (RMNH.CRUS.D. 47746) as well as in most specimens of the Taiwan N. minirostris material. In the largest male from Taiwan the subdistal tooth is distinct and acute. The anterolateral margin of the carapace in the holotype of N. minirostris is described as being ‘bluntly rounded’ and figured as such (Bruce & Bauer, 1997: fig. 2 A). In the paratype specimen of N. minirostris (RMNH.CRUS.D. 47746) as well as the Taiwan material however, a strongly produced anterolateral angle is present. Molecular data. The COI barcoding gene was compared with a subset of other sponge-associated pontoniine genera (Table I). No close similarity was found as genetic distances were more than 18 %. The morphologically very disimilar Thaumastocaris came up as the sister taxon in a phylogenetic analysis (fig. 10) indicating the distant relation to the other sponge-associated genera included in this analysis. Support for the branches within the ingroup is low.Published as part of Fransen, Charles H. J. M., 2013, A new species of the sponge-associated pontoniine shrimp genus Nippontonia Bruce & Bauer, 1997 (Decapoda, Caridea, Palaemonidae) from Sabah, Malaysia, pp. 343-357 in Zootaxa 3694 (4) on pages 345-355, DOI: 10.11646/zootaxa.3694.4.3, http://zenodo.org/record/21877
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
Expanding “Communities and Collections” in the K-State Research Exchange (K-REx) to benefit the K-State Community and Beyond
No full textKansas State University has used its institutional repository, the K-State Research Exchange (K-REx), to store and share its first year experience program, K-State First, and notably its common reading program, K-State First Book. We have done so with the aim that the accessibility and preservation of these documents ensures program stability, promotes engagement with first year programming, and provides the ability to foster growth,educational opportunities, and community building outside of K-State. Moving away from research concentrated repositories and taking a more holistic approach to scholarship, especially when realizing the pedagogical significance of collaborative campus programming, institutions can showcase, discover, preserve, and grow programs that shape campus communities and engagement.
This session will provide an overview of K-REx and spotlight the digital archive of the university’s first year experience program and common reading program, K-State First Book. We will discuss the benefits and challenges to expanding the purview of your repositories. We talkthrough the types of materials we decide to host in our repository and why we share what we do. We will also provide recommendations on new ways to evaluate what belongs in institutional repositories and how this diversity can benefit your program, your institution, the community, and others
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