218,867 research outputs found
Raw, not cropped supporting Western blot files for: Jeong YT. ... Pagano M. The ULK1-FBXW5-SEC23B nexus controls autophagy
No full textRaw, not cropped supporting Western blot files for:
Jeong Y., Simoneschi D., Keegan S., Melville D., Adler. N., Saraf A., Florens L., Washburn M., Casavotto C., Fenyo D., Cuervo A., Rossi M., and Pagano M.
The ULK1-FBXW5-SEC23B nexus controls autophagy.
eLife doi:7:e42253 doi: 10.7554, 2018
Notomastus koreanus Jeong, Soh, Wi & Suh 2018
No full text23. Notomastus koreanus Jeong, Soh, Wi & Suh, 2018 Notomastus koreanus Jeong, Soh, Wi & Suh, 2018: 146 –150, figs 2a–d, 3a–g. Type material: Holotype (MABIKNA00066337) Paratypes: (MABIKNA00146048, MABIKNA00146049). Type locality: China Sea, Korea, Busan, 35°6.33’N, 129°3.31’E, subtidal, sandy mud bottom, 16 m, October, 2011. Records: Only known from the type locality.Published as part of García-Garza, María Elena, León-González, Jesús Angel De & Tovar-Hernández, María Ana, 2019, Catalogue of Notomastus M. Sars, 1851 (Annelida, Capitellidae) and the description of a new species from the Gulf of California, pp. 249-273 in Zootaxa 4577 (2) on page 257, DOI: 10.11646/zootaxa.4577.2.2, http://zenodo.org/record/262970
Author Correction: Dynamic ice loss from the Greenland Ice Sheet driven by sustained glacier retreat (Communications Earth & Environment, (2020), 1, 1, (1), 10.1038/s43247-020-0001-2)
No full textThe original version of this Article contained an error in the spelling of the author Seongsu Jeong, which was incorrectly given as Seonsgu Jeong. This has now been corrected in both the PDF and HTML versions of the Article
Raw, not cropped supporting Western blot files for: Jeong YT. ... Pagano M. The ULK1-FBXW5-SEC23B nexus controls autophagy. eLIFE (2018).
No full textRaw, not cropped supporting Western blot files for:
Jeong Y., Simoneschi D., Keegan S., Melville D., Adler. N., Saraf A., Florens L., Washburn M., Casavotto C., Fenyo D., Cuervo A., Rossi M., and Pagano M.
The ULK1-FBXW5-SEC23B nexus controls autophagy.
eLife doi:7:e42253 doi: 10.7554, 2018
Ramp-rate limitation experiment using induced current method. Part 2: analysis
No full textThis paper describes an analysis of ramp-rate limitation experiments performed by a background magnet only without a power supply for the tested cable. Three-strand U-shape cable-in-cond nit conductor samples show distinctive ramp-rate limitation phenomena with sensitive transition between no-quench and quench results. Quench experimental results at various ramp rates are explained by a representative induced loop current model. Since the sample length is less than 1 m and the loop resistance through the joint is an order of 1 muOmega, the dominant loop current is induced mostly through the joint. Multiple quench-recovery processes during continuous magnetic field ramp are also explained due to fast recovery of the sample after quench. It is experimentally observed that the strand heat flux condition can be very influential to determine quench-recovery process near the critical heat flux regime of liquid helium. (C) 2003 Elsevier Ltd. All rights reserved
Tunable single-frequency ytterbium-sensitized erbium-doped fiber MOPA source with 150W (51.8 dBm) of output power at 1563 nm
Get PDFA single-frequency, single-mode ytterbium-sensitized erbium-doped fiber master-oscillator power-amplifier generated 150 W of continuous-wave output power at 1563 nm with 33% slope efficiency and was tuned in the range of 1546 to 1566 nm at >125 W
Dr. Duane M. Jackson, Morehouse College, July 2011
No full textThis video is a conversation with Dr. Duane M. Jackson. Dr. Jackson talks about his paper, "Recall and the Serial Position Effect: The Role of Primacy and Recency on Accounting Students' Performance." Jackie Daniel, AUC Woodruff Library, is the interviewer
Pleuroxus jejuensis Jeong, Kotov & Lee, 2013, sp.nov.
No full textPleuroxus jejuensis sp.nov. (Figs 2,3) Etymology. The taxon is named after its type locality, Jeju Island (South Korea). Type locality. A puddle in the Daseong wetland (260 m. a.s.l.), Jeju Special Self-Governing Province, Republic of Korea. Geographic coordinates: 33.4343 ºN; 126.7523 ºE (Table 1). Type material. Holotype. Parthenogenetic female, 0.45 mm, collected 29.11. 2012, NIBRIV0000264815. Paratypes. 3 females from the type locality, collected 29.11. 2012, NIBRIV0000264816; 3 females from the type locality, collected 29.11. 2012, NIBRIV0000264817; 20 females from the type locality, collected 14.02. 2012, MGU Ml- 124; the rest of numerous females from the type locality, collected 14.02. 2012, AAK-M- 2365 and collected 29.11. 2012, HGJ 339 a; 6 parthenogenetic females from Daseong stream itself (locality 2 in Table 1), collected 14.02. 2012, AAK-M- 2364. Diagnosis. Parthenogenetic female. Body yellow-brownish, relatively opaque, height about 0.8–0.9 body length, postero-ventral angle broadly rounded, without any teeth. Body moderately compressed laterally, in anterior view with regularly curved dorsum, top of carapace not ridged at all. Head shield wide, with maximum behind the level of mandibular articulation, postpore distance less than interpore distance. A row of minute setules at posterior valve margin located submarginally. Postabdomen wide, preanal margin longer than anal margin, preanal and postanal angle expressed, postanal margin somewhat longer than anal margin, dorso-distal angle widely rounded and prominent distally. Postanal teeth thin, organized in groups of two members in distal portion and 4–6 members in proximal portion of postanal margin. Proximal basal spine three quarters size of distal one. Antenna I with a well-defined basal peg and six distal spines. All apical "swimming" setae of antenna II, as well as basal and distal lateral seta of endopod subequal in size. Thoracic limb I with a short accessory seta, inner distal lobe with thin first seta. Filter plate of gnathobase II with eight setae, in few cases 7 setae; filter plate III with 8 setae; filter plate IV with 6, rarely 7 setae; filter plate V with 4 setae. Size up to 0.45 mm. Site Puddle in swampy area River (locality 2) Puddle in swampy area Remnants of the river (type locality) (type locality) (locality 2) Date 14.02. 2012 14.02. 2012 29.11. 2012 29.11. 2012 Collectors H.G. Jeong H.G. Jeong H.G. Jeong & A.A. Kotov H.G. Jeong & A.A. Kotov Latitude, N 33.4350 N 33.4342 33.4343 33.4348 Longitude, E 126.7518 126.7514 126.7523 126.7516 Description. Parthenogenetic female. General. Body yellow-brownish, relatively opaque. In lateral view body almost circular, high for the genus (body height/ body length about 0.8–0.9), maximum height in middle (Fig. 2 A). Dorsal margin evenly arched from tip of rostrum to postero-dorsal angle, which is ill-defined, posterior margin slightly convex, postero-ventral angle broadly rounded, without any teeth, ventral margin with a slight prominence in anterior half. Body moderately compressed laterally (Fig. 2 B), with regularly curved dorsum in anterior view, top of carapace is not ridged at all (Fig. 2 C). One to two parthenogenetic eggs in brood pouch. Head with a long rostrum, protruding downward and posterior (Figs. 2 A, D). Ocellus somewhat smaller than compound eye, lies closer to base of antenna I than to compound eye. Head shield wide, with maximum behind the level of mandibular articulation, with posterior margin rounded (Figs. 2 E–F), rostrum without a terminal tubercle. Two major head pores; postpore distance 0.7–0.8 interpore distance (Figs. 2 E–F). Lateral head pores minute, normally located symmetrically to midline (Figs. 2 G–H). Labrum with fleshy main body, small distal labral plate and a large medial labral keel, with well-defined apex, projecting beyond tip of rostrum (Fig. 2 D). Valves with subparallel lines at the antero-ventral portion (Figs. 2 A, I–J). Ventral margin armed with numerous setae of different size in different regions. The antero-ventral margin naked (Fig. 2 J), anteriormost portion of ventral margin with plumose setae, all located exactly at the margin; following setae (Fig. 2 J) naked and with spines at their bases; setae in middle and posterior half of ventral margin longer, lacking spines, plumose (Figs. 2 K). A row of minute setules at posterior valve margin located submarginally (Figs. 2 L). Postabdomen wide (Figs. 2 M–N), its ventral margin straight, preanal margin longer than anal margin, with a slight depression, anal margin concave, preanal angle prominent, postanal angle poorly expressed; postanal margin somewhat longer than anal margin, dorso-distal angle widely rounded and somewhat prominent distally; basis of claws bordered from postanal margin by a distinct depression (Fig. 2 N). Postanal teeth thin, organised in groups of two members in distal portion and 4–7 members in proximal portion of postanal margin, anal margin with a continuous row of fine setules. Laterally on postabdomen series of short, fine setules, normally distalmost fascicle containing slightly thicker setules. Postabdominal seta longer than preanal margin, with distal segment bearing long, rare setules (Fig. 2 N). Postabdominal claw approximately as long as anal margin, massive, evenly curved, with setules along ventral margin, and two basal spines, proximal one being in length three quarters of distal one (Fig. 2 O). Antenna I small, length/diameter = 2.5, narrowing distally, with a well-defined basal peg (Figs. 3 A–B). Antennular sensory seta slender, approximately as long as half the antenna I, arising from the middle, without any prominences. Nine short aestetascs of slightly differing size, with six spine-like projections around them. Antenna II (Fig. 3 C) relatively short, coxal part with two sensory setae (not represented in Fig. 3 C), basal segment robust, with a rudimentary distal spine. Antennal branches relatively elongated, endopod longer than exopod, all segments cylindrical, antennal formula, setae 0– 0–3 / 1 – 1–3, spines 1 – 0–1 /0– 0–1. All apical "swimming" setae, as well as basal and distal lateral seta of endopod, subequal in size. Spine on proximal segment of exopod short. Exopod and endopod apical spines subequal in size (Fig. 3 C). Maxilla I as a hillock with three setulated setae (Fig. 3 D). Trunk limb I (Figs. 3 E–F). Distal portion of limb corm with a short accessory seta (Fig. 3 F, pointed with arrow), outer distal lobe (Fig. 3 F, ODL) bears a long terminal seta with distal segment unilaterally armed with minute setules, and a short naked lateral seta. Inner distal lobe (Fig. 3, IDL) with a fine, naked first seta, second and third setae subequal in size and similarly armed distally with short setules. Endite 3 with three posterior setae subequal in size (Fig. 3 E, a–c) and somewhat longer setulated anterior seta with a small sensillum near its base (Figs. 3 E & G, marked by 1). Endite 2 with three posterior setae (Fig. 3 E, d–f), and thin anterior seta (pointed with arrow, number 2) bilaterally armed with short setules distally (Fig. 3 H), a small sensillum near the latter. Endite 1 with thin posterior setae g–i, a short seta j, and anterior seta (with number 3) (Fig. 3 I), subequal in size with seta 2. Fascicles of thin setules on inner face of limb, plus bunches of longer, thicker setules arranged in five rows at ventral margin. Two ejector hooks, subequal in size. A remnant of maxillar process (Fig. 3 E, MPR) with a single seta. Trunk limb II (Figs. 3 J–K). Exopodite small, subquadrangular, with a short seta. Inner portion of limb with eight scrapers (Fig. 3 J, 1–8), 1–2 longer and armed with fine setules, others armed distally with thin spinules, setae 6–8 the shortest. A system of small projections posteriorly to scrapers 1–4, and a small sensillum near scraper 4. Distal armature of gnathobase with a bunch of setules and four setae (Figs. 3 K), a bunch of setules distally to seta 1, and a bunch of fine setules basally. Filter plate II with eight setae, in few cases 7 setae. Trunk limb III (Figs. 3 L–M). Exopodite sub-rectangular, with four distal setae (Fig. 3 L, 1–4) and three plumose lateral setae (5–7). Distal endite with three anterior setae (Fig. 3 M, 1–3), basalmost seta (3) stouter and shorter, small sensillae near bases of setae 2 and 3. Basal endite with four anterior setae (Fig. 3 M, 4–7), slightly increasing in size basally, armed with fine setules distally, a small sensillum near seta 4. On posterior surface, six soft setae (Fig. 3 L, a–f), bilaterally armed with fine setules. Gnathobase not clearly separated from basal endite. Distal armature of gnathobase with a large, bottle-shaped sensillum, three setae, and a bunch of setules (Fig. 3 M), filter plate III with eight setae. Trunk limb IV (Figs. 3 N–O). Pre-epipodite rounded, setulated; epipodite ovoid (not represented in Fig. 3 N); exopodite wide, subovoid, with seven setae of unequal size (Fig. 3 N, 1–7). Inner-distal portion of limb IV with four marginal setae (Fig. 3 O, 1–4). Distalmost seta (Fig. 3 O, 2) short and stout, all setae setulated distally, with thick distal segments, a sensilla located near each setae 2 and 3. On posterior surface, four soft setae (Figs. 3 N, a–d). Distal armature of gnathobase with four setae (Fig. 3 N), filter plate with six, rarely seven setae. Trunk limb V (Fig. 3 P). Pre-epipodite setulated; epipodite subovoid, exopodite large, subovoid, with a single distal seta 1 and three lateral setae (2–4), distally to seta 1 there are two projections bearing long setules. Inner limb portion as elongated, flat lobe, with setulated inner margin, supplied with two setulated setae (Fig. 3 P, 1 and 2). Distal armature of gnathobase as a single projection, filter plate V with four long, naked setae. Size. 0.23–0.45 mm. Ephippial female, male. Unknown. Distribution and Ecology. Up to date, P. j e j u e n s i s sp. nov. is known from two close localities on Jeju Island. No similar species were found in nearest regions of China (Chiang & Du 1979), Far East of Russia (Kotov et al., 2011 a–b), Japan (Uéno 1926, 1937; Tanaka 1994) and continental South Korea (Kotov et al. 2012). The species seems to be endemic of this island. The information on localities is given in Tables 1–2. It is remarkable, that at two different dates P. jejuensis sp.nov. occurred both in the river and in the puddles from the swampy area. It means that it could be present in water bodies of different type. In November it co-occurred with six other species of cladocerans in stony pools (remnants of the almost dried Daseong river, Fig. 1 F). Unfortunately, our sampling covered only the winter season, no data are available on these localities in summer, i.e. at the monsoon time. Site Puddle in swampy area River Puddle in swampy area Remnants of the river Date 14.02. 2012 14.02. 2012 29.11. 2012 29.11. 2012 Simocephalus cf. vetulus (O.F. Müller) + Scapholeberis kingi Sars + Bosmina longirostris (O.F. Müller) + Acroperus harpae (Baird) + Alona costata Sars + Alonella cf. exigua (Lilljeborg) + Alonella excisa (Fischer) + Cyclopoida undet. + + + +Published as part of Jeong, Hyun Gi, Kotov, Alexey A. & Lee, Wonchoel, 2013, A new species of the genus Pleuroxus Baird (Cladocera: Anomopoda: Chydoridae) from Jeju Island, South Korea, pp. 31-40 in Zootaxa 3666 (1) on pages 33-38, DOI: 10.11646/zootaxa.3666.1.3, http://zenodo.org/record/28383
A combinatorial approach to solution-processed InGaO3(ZnO)M superlattice films: Growth mechanisms and their thermoelectric properties
No full textMulticomponent amorphous InGaZnO thin films with several metal cations have been synthesized with flexible chemical composition control based on a sol-gel process, and a combinatorial approach through a sol-gel process enables us to perform a systematic survey to fluently find the best film properties. Contrary to amorphous films, crystalline InGaO3(ZnO)m requires a refined chemical composition ratio among metal cations. These ratios are expected to affect the growth evolution and thermoelectric properties of two-dimensional InGaO3(ZnO)m superlattice structures with various compositional combinations. Here, we explore a combinatorial approach to the ratio of metal cations using various mole fractions of metal precursors in InGaZnO sol for amorphous InGaZnO films fabricated on an epitaxial ZnO buffer layer, and then, they were crystallized with various chemical compositions. The crystallized InGaO3(ZnO)m films can be classified as strong single-phase InGaO3(ZnO)m, double-phase InGaO3(ZnO)m/InGaO3(ZnO)m+1, and weak single-phase InGaO3(ZnO)m with excess metal ions. Among them, the strong single-phase InGaO3(ZnO)m films with superlattice structures showed superior thermoelectric power factors. The detailed microstructural growth evolution of single- and double-phase InGaO3(ZnO)m films was investigated using transmission electron microscopy. © The Royal Society of Chemistry 20163
"Reflections on the subject of Emigration from Europe with a view to Settlement in the United States" By M. Carey.
No full text"Reflections on the subject of Emigration from Europe with a view to Settlement in the United States: containing bried sketches of the moral and political character of those states.
By M. Carey, member of the American philosophical, and of the American Antiquarian Society, and author of The Olive Branch, Cindiciae Hibernicae, essays on banking, on political economy, and on internal improvement.
To which are now added the English editor's comments on the subject; together with Important Advice to Emigrants, and Cautions Against Impositions Practiced in the Outports
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