126,591 research outputs found
Chitosan Coating Enriched With Ruta graveolens L. Essential Oil Reduces Postharvest Anthracnose of Papaya (Carica papaya L.) and Modulates Defense-Related Gene Expression
No full textAnthracnose of papaya (Carica papaya L.) caused by the fungus Colletotrichum spp. is one of the most economically important postharvest diseases. Coating with chitosan (CS) and Ruta graveolens essential oil (REO) might represent a novel eco-friendly method to prevent postharvest anthracnose infection. These compounds show both antimicrobial and eliciting activities, although the molecular mechanisms in papaya have not been investigated to date. In this study, the effectiveness of CS and REO alone and combined (CS-REO) on postharvest anthracnose of papaya fruit during storage were investigated, along with the expression of selected genes involved in plant defense mechanisms. Anthracnose incidence was reduced with CS, REO, and CS-REO emulsions after 9 days storage at 25°C, by 8, 21, and 37%, respectively, with disease severity reduced by 22, 29, and 44%, respectively. Thus, McKinney’s decay index was reduced by 22, 30, and 44%, respectively. A protocol based on reverse transcription quantitative real-time PCR (RT-qPCR) was validated for 17 papaya target genes linked to signaling pathways that regulate plant defense, pathogenesis-related protein, cell wall-degrading enzymes, oxidative stress, abiotic stress, and the phenylpropanoid pathway. CS induced gene upregulation mainly at 6 h posttreatment (hpt) and 48 hpt, while REO induced the highest upregulation at 0.5 hpt, which then decreased over time. Furthermore, CS-REO treatment delayed gene upregulation by REO alone, from 0.5 to 6 hpt, and kept that longer over time. This study suggests that CS stabilizes the volatile and/or hydrophobic substances of highly reactive essential oils. The additive effects of CS and REO were able to reduce postharvest decay and affect gene expression in papaya fruit
The Ordovician succession from the western Iberian Ranges (NE Spain): a review with new data
No full text8 páginas, 2 figuras.-- Edited by: G. L. Albanesi / M. S. Beresi / S. H. Peralta.-- Proceedings of the International Symposium on the Ordovician System. San Juan - Argentina 2003.Our work was carried out within the framework of the Project BTE2000–1310 (Bioestratigrafía y correlación del Paleozoico Inferior de la Rama Castellana de la Cordillera Ibérica), Spanish Ministry of Science and Technology.Peer reviewe
Parastygocaris Noodt 1963
No full textGenus Parastygocaris Noodt, 1963 Diagnosis (Noodt 1970: 228). Stygocarididae with one-segmented exopod on thoracopods 2–6 (=pereopods 1–5). Flagella of A 1 and A 2 composed of a relatively large number of articles. Rostrum square, tongue-shaped. Ur exopod bisegmented. Type species: Parastygocaris andina Noodt, 1963 Others species: P. goerssi Noodt, 1963; P. c l a p s i Grosso & Peralta, 1997; P. schminkei Grosso & Peralta, 1997.Published as part of Peralta, Marcela, 2014, A new stygobitic species of Stygocarididae (Crustacea: Anaspidacea) from South America, pp. 396-408 in Zootaxa 3760 (3) on page 397, DOI: 10.11646/zootaxa.3760.3.6, http://zenodo.org/record/22858
Parastygocaris luisgrossoi Peralta, 2014, n. sp.
No full textParastygocaris luisgrossoi n. sp. Type Locality: stream tributary of Río de la Carpa, northern sector of Río Quinto basin, Sierra de San Luis, San Luis Province, Argentina. 32 º 50 ’ S; 65 º 59 ’ W, 1491 m above sea level. Type specimens: Holotype male (FML-CRUST01109). Paratypes: five females (FML- CRUST 01110), five males (FML-CRUST01111). All collected at type locality, 6 -December- 2012, Col. M. Peralta, hyporheic zone. Additional specimens examined (FML-CRUST01112): one male, four females and three immatures, same data as holotype. Accompanying fauna: Hydra, Nematoda, Nematomorpha, Oligochaeta, Acari, Diptera (Staphylinidae and Ceratopogonidae, larvae), Collembola, Ostracoda, Amphipoda Ingolfiellidea, Isopoda Protojaniridae, Copepoda Harpacticoida (Parastenocarididae) and Cyclopoida. Description of Holotype. Total length 1.7 mm. Body moderately chitinized, all somites (seven pereomeres and six pleomeres) of similar size. Cephalothorax and all body somites with one or two thin simple dorsal setae at each side; second to sixth pleonites with one simple ventral seta at each side, those on second pleonite p l a c e d near to corresponding pleopod protopod; lateral margins of second to fifth pleonites (Fig. 1 a) each with one plumose seta (type IB 1). Rostrum (Fig. 1 b) trapezoidal, with blunt end and one simple seta on each lateral margin. A 1 (Figs. 1 b, c) peduncle three-segmented, OF with nine and IF with three articles. First segment of peduncle longer than the two following segments combined, with longitudinal ridge on dorsal surface; two dorsal plumose setae (type IB 1) placed near statocyst cavity; inner margin with transverse row of four–five simple setae; outer margin with lateral setiferous group composed of three subdistal plumose setae (type IB 1). Second segment wider than long, outer margin with weak lateral expansion bearing three plumose setae (type IB 1); dorsal surface with oblique row of six recurved ringed setae (Fig. 5 a) of increasing length towards distal. Third segment widened at distal end, where the two flagella are articulated; dorsal surface with one simple seta on bifurcation of both flagella; inner margin with two simple setae; distolateral angle with one plumose seta (type IA 1). OF slightly curved due to morphology and articulation of proximal articles; first article wide, with inner margin slightly serrated (visible in Fig. 1 b); bearing four short plumose setae (type IA 1) (=”Sinnesorgan” Schminke 1974); second article medial margin globoid, with a deep longitudinal depression (visible in Fig. 1 d). Distal margin of third to seventh articles each with one or two aesthetascs and one–four simple setae. Ninth article with one aesthetasc and five simple setae, of which three short and two longer. IF with three articles, first article short and wide, distomedial angle with three setae (two long and one short), distolateral angle with one plumose and long seta (type IA 1), dorsal surface with a transverse row of three thin short setae; second article articulating dis to- la terally to preceding article, inner margin with one recurved seta bearing fine setules on one side of shaft (Fig. 1 b); third article with six simple or plumose (type IA 1) setae. A 2 (Fig. 1 e) attaining 3 / 5 of A 1 length, with four-segmented peduncle and five-articulate flagellum; peduncle segments two to four longest, their combined length equalling flagellum length. Inner margin of third segment with three middle setae: two short plumose (type IB 1), and one long simple; distomedial angle with three simple setae; outer margin with two lateral setae, one plumose (type IB 1), and one simple. Surface of fourth segment with a transverse row of four distal, simple setae, and two groups of simple setae along inner margin: one, proximal, comprising two setae, other of four setae; outer margin near distal angle with two plumose setae (type IB 1), one very long, and one short; distomedial angle with two simple setae. Proximal article of flagellum with one simple seta on distomedial angle; articles two to four each with six–eight distal setae, simple or plumose, those on distal margin longest. Terminal article with five simple setae on tip. Labrum (Fig. 2 a): wide, with distal margin slightly excavated; anterior edge and dorsal surface with acuminate microsetae. Left Md (Fig. 2 b) pars incisiva with nine conical teeth in palisade arrangement, t h e d i s t a l o n e in a plane perpendicular to remaining teeth; diastema with two serrated setae (type IIB 1); margin of molar process with one spiniform process; molar process high, grinding surface surrounded by many tiny denticles. Right Md (Fig. 2 c) similar to left counterpart, pars incisiva with six teeth in palisade on distal curved edge: three most proximal smaller; diastema with only one serrated seta; molar process without spiniform process. Paragnaths with oval lobes (Fig. 2 d); inner edge and distal margin of each lobe with long, thin acuminate microsetae. Mx 1 (Fig. 2 e): consisting of two endites, inner one globoid and shorter, with four strong, pappose (type IA 2) setae; with lateral and ventral acuminated microsetae. Oblique end of outer endite bearing nine setae, innermost setulodenticulate (type IA 4), rest arranged in double row of denticulate (type IIIA 1) or setulodenticulate setae. Mx 2 (Fig. 2 f) with four endites (the fourth or distal endite partially subdivided), all with a doble row of distal setae; first endite bearing 13 setae: five distal plumose (type IA 1), eight lateral arranged in a row, pappose (type IA 2) with short setules; second endite with four distal setae (three setulodenticulate type IA 4, one plumose type IA 1); third and fourth endites each with five long distal setae (two simple, two setulate type IA 3, one setulodenticulate type IA 4); fourth endite also with one subdistal short outer seta. Mxp (Fig. 2 g) strong, seven-segmented, lacking exopod or epipodites. Coxa wide, with endite reaching half the length of basis, with nine setae: six distal (Fig. 5 c), of which five are pappose with setules and setuletes (type IA 2), and one (innermost) is simple (type IIA 1); other three pappose setae (type IA 2) placed along inner margin, next to base of endite. Basis expanded, inner margin with a double row of 17 setae comprising plumose (type IA 1) and simple setae intercalated. Ischium, dis tom edial angle with two plumose (type IA 1) setae and two ventral, simple setae implanted close to the latter. Merus, inner margin with six plumose (type IA 1) setae; ventral surface of segment with four plumose (type IA 1) or simple setae. Carpus narrowest and shortest segment, both margins with one plumose seta (type IA 1). Propodus, both dorsal and ventral surface with two plumose (type IA 1) obliquely aligned setae, with setules and setulette on the setal shaft (Fig. 5 d); distomedial and distolateral angles with plumose setae (type IA 1), and one seta midway of outer margin. Dactylus armed with two strong claws and one thin simple seta. Pereopods, all seven-segmented. P 1 (Fig. 3 a) slightly shorter and wider than rest, P 2 –P 7 (Figs 3 b–g) similar in size; P 1 –P 6: with two oval epipodites; P 1 –P 5: basis with one-segmented cylindrical exopod bearing two long plumose setae (type IA 1). P 7 lacking exopod and epipodites, directed forwards. Chaetotaxy of all pereopods comprising simple or plumose setae (type IA 1), basis, ischium and merus with one-two distal simple or plumose setae, carpus with one (the posterior) or two (both anterior and posterior) plumose setae, P 1 and P 7 propodus with two plumose aligned setae on posterior margin, P 2 –P 6 propodus with only one seta. P 1 dactylus with two strong claws, rest with a single claw. P 6 coxa bearing one anterior, thin simple seta. Pleopods 1–2 transformed into petasma, both directed forwards. Pl 1 (Figs 4 a–b) biramous with wide protopod, rami indistinctly articulated with protopod; endopod rigid, triangular, shorter than exopod, with four spiniform processes on tip: one terminal, other three curved backwards; inner margin of protopod with two coupling setae (type IIIA 2); exopod of alveolar aspect, wide, globose; middle internal area on both rami with microsetae. Pl 2 (Fig. 4 c) uniramous, styliform, two-segmented, segments similar in length; protopod bearing two or three coupling setae on distal third of inner margin; distal segment with an external lamella encompassing two thirds of distal part, covered with tiny spiniform processes and with serrated edges. Uropod (Fig. 4 d): protopod longer than wide, with aligned lateral setae on both margins, inner row consisting of eight plumose setae (type IA 1); outer row with three pappose setae (type IA 2), distalmost longest. Endopod and exopod equal in length. Exopod two-segmented, proximal segment slightly longer than protopod and as long as 2 ½ times length of distal one; segment prov ided with five pappose setae (type IA 2) on external margin; internal margin with one proximal small simple seta and three distal pappose (type IA 2), stronger setae. Distal segment with seven pappose (type IA 2), very long setae. Endopod one-segmented, lined with 15 setae, of which seven on inner margin shorter; all setae plumose; dorsal surface of seg m ent with seven plumose setae (type IB 1), two of which very long and strong, remaining short and smaller. Telson (Fig. 4 e) 1.4 times wider than long. Anal operculum slightly convex and extending almost until tip of lateral lobes, with one or two simple small setae at each side. Lateral lobes each with three card setae (type IIB 2), of which middle one strongest, plus one or two simple tiny setae. Description of female Paratype FML-CRUST01110d. Total length: 1.69 mm (excluding antennae). A 1 OF with nine and IF with three articles (Fig. 1 f), A 2 with four-segmented peduncle and five-articulate flagellum (Fig. 1 g), pleopods absent. Morphology and chaetotaxy of body and appendages similar to holotype except for some characters of antennae, P 1, P 6 and Ur as detailed: second segment of A 1 peduncle with two dorsal plumose setae (type IA 1) (holotype with oblique row of six ringed setae); A 1 OF straight, basal articles similar to each other (without the curvature or depression present in the A 1 of holotype), third article without aesthetascs; A 1 IF articles narrower and with inner setae smaller than in holotype, the second one with two thin simple setae on inner margin (without the pappose seta present in holotype); A 2 fourth segment with three plumose setae near distal external angle (two in holotype), first article of flagellum without setae (one in holotype); P 1 propodus with three plumose aligned setae on posterior margin (two in holotype); P 6 (Fig. 3 h) basis with one long plumose medial seta on inner margin (absent in holotype) and two anterior simple setae on coxa; Ur protopod, inner margin with seven aligned plumose setae (eight in holotype), proximal segment of exopod with four pappose setae on external margin (five in holotype). Telson and mouthparts as in holotype. Variability. Mean length was 1.97 mm for five male paratypes and 1.75 mm for five female paratypes. Maximum length was 2.4 mm for males and 1.90 mm for females. Males: some variations were observed in the number of articles and chaetotaxy of outer flagellum of A 1, claw of Mxp, chaetotaxy of P 1 and P 6: in some males (length between 1.86–2.4 mm): A 1 OF with 10 articles (nine in the holotype); peduncle chaetotaxy: first article, with transverse subdistal row of five setae (four in the holotype); second article, dorsal oblique row of five ringed recurved setae (six in the holotype). In one male, the dactylus of Mxp was armed with only one claw. We observed males with three plumose aligned setae on posterior margin of P 1 propodus (two in holotype) and two distal setae on P 6 merus (one in holotype). In two females (lengths 1.9 mm and 1.6 mm), the A 1 IF had only two articles. Etymology. The new species is named in honor to Dr Luis E. Grosso, Fundación Miguel Lillo-CONICET (Tucumán-ARGENTINA), one of the pioneers of biospeleology in Argentina. Diagnosis of Parastygocaris luisgrossoi n. sp. The new species is distinguished by the following combination of characters: Antennule outerr flagellum with nine (in females) or 9–10 (in males) articles and inner flagellum with three (in males) or two–three (females) articles. In both sexes antenna with four-segmented peduncle and fivearticulate flagellum. Maxilla setiferous row of eight pappose setae along inner margin of internal endite. Maxilliped basis inner lobe with 17 setae arranged in a double row. Uropod protopod, inner margin with seven–eight plumose setae; endopod with a total of 15 marginal setae, seven of which on the inner margin; exopod, distal segment lined by seven pappose setae. Petasma: pleopod 1, inner ramus triangular, stiff, tip with spiniform processes and coupling setae. Pleopod 2 styliform, with two segments of similar length; distal segment with an external lamella and serrated edges. Secondary sexual characters: Male: antennule, second article of peduncle with an oblique row of five–six recurved ringed setae; outer flagellum with basal part slightly curved due to morphology and articulation of its articles, second article globular, with internal depression; second article of the inner flagellum articulating disto-laterally to preceding article. Female: pereopod 6 with one long and strong plumose seta on basis. Systematic comments. The Stygocarididae are the most differentiated anaspidacean family, and the sister group of Patagonaspididae (Schminke 1975; Schram 1984; Grosso & Peralta 2002). A morphological simplification of appendages (short antennae; Md, Mx 1, Mx 2 each devoid of palp; Mxp without epipodites or exopod; exopods of pereopods one-segmented or absent; pleopods vestigial or absent) is evident in both families, and especially marked in the species of Stygocarididae. The Stygocarididae includes four genera: Parastygocaris Noodt, 1963, Stygocaris Noodt, 1963, Stygocarella Schminke, 1980, and Oncostygocaris Schminke, 1980. An analysis of the diagnosis of Parastygocaris (Noodt 1970) shows that the one-segmented cylindrical exopod on P 1–5 represents its only generic distinctive feature, the rest of characters mentioned as dia g nos tic being shared with some Stygocaris species. The only known species of Patagonaspididae, Patagonaspides sandroruffoi Grosso & Peralta, 2002 shares with Parastygocaris the presence of one-segmented exopods on P 1–5; however, both genera differ in the structure of the exopod: it is cylindrical with 2 setae in Parastygocaris whereas truncated and ribbon-shaped, with 8 setae in Patagonaspides Grosso & Peralta, 2002. When comparing Parastygocaris luisgrossoi n. sp. with related taxa species, we considered the following characters: rostral morphology; articles and secondary sexual characters of antennae; features of the pleopods; and chaetotaxy of Mx 2, Mxp, Pl, and Ur (Table 1). The new species is similar to P. g o e rs s i by several characters: number of articles of A 1 OF; A 1 IF of male with secondary sexual characters; number of inner setae on the first endite of Mx 2; number of marginal setae on Ur protopod; and morphology of the rostrum. P. luisgrossoi n. sp. shares with P. c l a p s i the number of setae on the Mxp endite and the chaetotaxy of the Pl 1 inner ramus. Regarding pleopod morphology, all Parastygocaris species are greatly similar except for P. clapsi due to its trisegmented Pl 2. Within the genus Parastygocaris, the new species is small (1.97 mm mean length for males; 1.75 mm for females) taking into account that P. andina, the largest Stygocarididae species, exceeds 4 mm long. Besides being the largest species, P. andina has several unique characters: it has the longest A 1 and the greatest number of cuticular extensions in many appendages (Mx 2, pereopods, Pl 2, Ur). Comments on setal types. The study of the chaetotaxy of Parastygocaris luisgrossoi n. sp. under optical and electron microscopy has allowed the distinction of a new type of ringed seta as well as 15 types of previously described cuticular extensions (Peralta 2010): - Macrosetae Type I: with infracuticular articulation (IA 1: plumose; IA 2: pappose; IA 3: setulate; IA 4: setulodenticulate a and setulodenticulate b); and with supracuticular articulation (IB 1: plumose) - Macrosetae Type II: shaft smooth (IIA 1: simple; IIA 3: aesthetasc); and with denticles (IIB 1: serrate; IIB 2: card) - Macrosetae Type III: with denticles (IIIA 1: denticulate; IIIA 2: coupling seta); and without denticles, strong (IIIB) - Microseta Type A: acuminate - Spiniform processes The new species shows a remarkable enhancement of the sensory function of the male A 1, where a new seta type, here called ringed, occurs and which had not been detected before in any Stygocarididae species. This element is a macroseta with infracuticular articulation (type I), circular in cross-section, characterized by parallel tenuous rings around the shaft and one fringe of multiple fine short setules arising from the shaft wall (Fig 5 a). An oblique row of five–six of these recurved setae occurs only on the dorsal surface of the second segment of the peduncle of A 1. These setae resemble those inserted on the A 1 IF of Anaspides tasmaniae Thomson, 1 8 9 3, an exclusively male character. However, in A. tasmaniae, these setae do not bear setules on the shaft, but small scale-like plates. In addition, the A 1 IF of the male of Parastygocaris luisgrossoi n. sp. has a recurved seta with fine setules on one side of its shaft; thus, this setal type is a special type of pappose seta (type IA 2). In the Mxp, an appendage subjected to high mechanical stress, the cluster of robust distal setae of the coxal endite includes only one simple seta (type IIIB) (Fig. 5 c), whereas the rest are pappose. This simple seta is placed on the inner angle of the endite. Further detailed studies of other Stygocarididae species are necessary to ascertain whether this character is an autapomorphy. Biogeographic remarks. The evolution of the Anaspidacea is believed to have occurred only on their Gondwanan refugium (Schram & Hessler 1984). Stygocaris (Stygocarididae) has a disjunct geographical distribution in Australia, New Zealand, and South America (Chile- Argentina). This link across the southern Pacific is a manifestation of an ancient dispersal pathway, or alternatively a vicariant track, that included Antarctica when Gondwana was intact (Schram 2008), and thus, the generic differentiation w i thi n the fa m ily must have occurred at least before the Cretaceous (Grosso & Peralta 2002), when the breakup of Gondwana accelerated, and before the uplift of the South American Andes. The new Stygocarididae species, was collected at the southern Sierra de San Luis (Fig. 6), a unit that is part of the eastern Sierras Pampeanas characterized by a base of Precambrian to Paleozoic rocks, partially covered by younger sequences (Brodtkorb et al. 2009). Some geologists consider that the Sierras Pampeanas represent one of the fragmented remnants of Gondwanan paleosurfaces, geomorphological systems that were generated when the former Gondwana super-continent was still in place and whose preservation was possible due to similar tectonic conditions in the drifting fragments (Rabassa et al. 2010). The rise of the Andes was a pivotal event for the ancient freshwater biota of the region, because it created the current Magdalena and Paraguay Rivers and most of the Orinoco System, produced changes in former river courses (Lundberg et al. 1998, Potter 1997), and also created new upland habitats (eg. Sierras Pampeanas intermountain valleys). All these events must have influenced the modern pattern of distribution of the stygobitic Stygocarididae in South America; in addition, the region was affected by repeated marine incursions from the Pacific, South Atlantic and Caribbean since Paleozoic times. All these happenings are potential vicariant events for groundwater biotas.Taking into account the above mentioned factors, as well as the long evolutionary history of Anaspidacea, we postulate the probable existence of an ancient groundwater basin in what is now the intermountainous valleys of western South America south of 28 ºS, which would have harboured interstitial fauna of great and diverse antiquity. The ocurrence of Ingolfiellidae amphipods, a group that presumably dates from at least Triassic times (Vonk & Schram 2003), and of Gondwanan Protojaniridae isopods as accompanying fauna of the new Parastygocaris species, supports this hypothesis.Published as part of Peralta, Marcela, 2014, A new stygobitic species of Stygocarididae (Crustacea: Anaspidacea) from South America, pp. 396-408 in Zootaxa 3760 (3) on pages 397-406, DOI: 10.11646/zootaxa.3760.3.6, http://zenodo.org/record/22858
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
Toma de decisiones y su influencia en la rentabilidad financiera, empresa Peralta Motors E.I.R.L. año 2015
No full textLa Tesis titulada “Toma de decisiones y su influencia en la rentabilidad financiera,
empresa Peralta Motors E.I.R.L. año 2015”; tiene como objetivo principal
determinar la influencia de la toma de decisiones en la Rentabilidad, de la
Empresa Importaciones Peralta E.I.R.L.
La muestra tomada para el desarrollo de la investigación, fue de 7 trabajadores de
la empresa Importaciones Peralta E.I.R.L., conformada por el gerente, una
secretaria y cinco vendedores.
El problema identificado es la deficiente toma de decisiones por falta de
información adecuada. Esta problemática se expresa en la siguiente pregunta:
¿Cuáles son las deficiencias en la toma de decisiones y su influencia en la
Rentabilidad Financiera de la empresa Importaciones Peralta E. I. R. L?, ante la
problemática se propone la solución a través de la formulación de la hipótesis: La
toma de decisiones es deficiente e influye negativamente en la Rentabilidad
Financiera, en la Empresa importaciones Peralta EIRL. Este trabajo se ha
orientado al siguiente objetivo: Determinar la influencia de la toma de decisiones
en la Rentabilidad, de la Empresa Importaciones Peralta E.I.R.L. La investigación
es básica, pero las teorizaciones efectuadas pueden ser aplicadas para tomar las
decisiones efectivas, la investigación es del nivel descriptivo. El diseño es no
experimental.
De los resultados obtenidos, se concluyó que la toma de decisiones realizada por
los trabajadores de la empresa Importaciones Peralta E.I.R.L. sí influye en la
rentabilidad de la empresa
Square Dancing with the Stars to Enhance Dynamic Hirschman Linkages?
No full textIn this Presidential Address, the author takes the reader on a reconnaissance of his life and time as a regional scientist. He points out scenery he found scintillating along the way, hoping that some may pick up the banner and chew on a few of the ideas for a while. He suggests a revisit to Albert O. Hirschman’s notion of key sectors and more empirical analysis related to Marcus Berliant’s and Masahisa Fujita’s notion of knowledge creation and transfer.Presidential Address, San Antonio, Texas, March 29, 2014 (53rd Meetings of the Southern Regional Science Association
Inner Derivations and Weak-2-Local Derivations on the C*-Algebra C-0(L, A)
No full text[EN] Let L be a locally compact Hausdorff space. Suppose A is a -algebra with the property that every weak-2-local derivation on A is a (linear) derivation. We prove that every weak-2-local derivation on is a (linear) derivation. Among the consequences we establish that if B is an atomic von Neumann algebra or a compact -algebra, then every weak-2-local derivation on is a linear derivation. We further show that, for a general von Neumann algebra M, every 2-local derivation on is a linear derivation. We also prove several results representing derivations on and on as inner derivations determined by multipliers.Jorda Mora, E.; Peralta, A. (2017). Inner Derivations and Weak-2-Local Derivations on the C*-Algebra C-0(L, A). Integral Equations and Operator Theory. 89(1):89-110. https://doi.org/10.1007/s00020-017-2390-xS89110891Akemann, C.A., Elliott, G.E., Pedersen, G.K., Tomiyama, J.: Derivations and multipliers of C ∗ -algebras. Am. J. Math. 98(3), 679–708 (1976)Akemann, C.A., Johnson, B.E.: Derivations of non-separable C ∗ -algebras. J. Funct. Anal. 33, 311–331 (1979)Akemann, C.A., Pedersen, G.K., Tomiyama, J.: Multipliers of C ∗ -algebras. J. Funct. Anal. 13, 277–301 (1973)Archbold, R.J.: On the norm of an inner derivation of a C ∗ -algebra. Math. Proc. Camb. Philos. Soc. 84, 273–291 (1978)Archbold, R.J., Somerset, D.W.B.: Inner derivations and primal ideals of C ∗ -algebras. II. Proc. Lond. Math. Soc. (3) 88(1), 225–250 (2004)Ayupov, S., Arzikulov, F.N.: 2-Local derivations on algebras of matrix-valued functions on a compact, preprint (2015). arXiv:1509.05701v1Ayupov, Sh, Kudaybergenov, K.K.: 2 -local derivations on von Neumann algebras. Positivity 19(3), 445–455 (2015). doi: 10.1007/s11117-014-0307-3Burgos, M., Cabello, J.C., Peralta, A.M.: Weak-local triple derivations on C ∗ -algebras and JB ∗ -triples. 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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
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